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CAS No. : | 634-67-3 | MDL No. : | MFCD00042819 |
Formula : | C6H4Cl3N | Boiling Point : | - |
Linear Structure Formula : | - | InChI Key : | RRJUYQOFOMFVQS-UHFFFAOYSA-N |
M.W : | 196.46 | Pubchem ID : | 12464 |
Synonyms : |
|
Signal Word: | Danger | Class: | 6.1 |
Precautionary Statements: | P273-P280-P301+P310+P330-P311 | UN#: | 2811 |
Hazard Statements: | H301+H311+H331-H373-H410 | Packing Group: | Ⅲ |
GHS Pictogram: |
* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
82% | Stage #1: 2,3,4-trichloroaniline With hydrogenchloride; sodium nitrite In water at -5 - 5℃; for 1h; Stage #2: With copper(l) chloride In water at 50 - 80℃; for 1h; | 3 Preparation of intermediate 1,2,3,4-tetrachlorobenzene (IV) In a 500 ml bottle 2,3,4-trichloroaniline 10 g (0.051 mol) and concentrated hydrochloric acid 21 g were added. The temperature was controlled to -5-5°C by adding 4 g of aqueous solution of sodium nitrite. After completion of addition, the mixture was insulated for 1 hour. In another 1000 ml bottle 50 g concentrated hydrochloric acid and 6 g cuprous chloride were added at 50°C and the preceding nitrosation solution was added, and heated to 80°C for 1 hour. Then the mixture was cooled to 30 ° C, extracted with dichloroethane, and evaporated to dryness to obtain 1,2,3,4-tetrachlorobenzene 9 g, GC analysis (more than 98%) yield of 82%. |
Diazotization; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
83% | With iron; ammonium chloride In water; 1,2-dichloro-ethane for 2h; Reflux; | 2 Preparation of intermediate 2,3,4-trichloroaniline (III) In a 500 ml four-necked flask, 8 g of iron powder (0.14 mol), 80 g of dichloroethane,100 g water and 2 g ammonium chloride were added, and refluxed. 2,3,4-trichloronitrobenzene 11.5 g (0.051 mol) was added dropwise to a solution of 20 g of dichloroethane. After completion of the addition, the mixture for insulated for 2 hours and GC analysis was carried out. After completion of the reaction, the reaction mixture was filtered, the filtrate was washed with water, layered, organic phase was combined and the solvent was dried to obtain 8.2 g finished product. Yield 83%. |
With hydrogenchloride; tin | ||
With hydrogen In methanol at 20℃; for 1h; chemoselective reaction; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With hydrogenchloride at 180℃; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With diphenylether Hydrolysis.mit wss. Natronlauge, Erh. mit Diphenylaether auf 275grad, Beh. des Rktprod. mit Phosphorylchlorid; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
93% |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With N-ethylmorpholine;; copper diacetate In N,N-dimethyl-formamide at 145℃; for 3h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With sulfuric acid; acetic acid; potassium iodide; sodium nitrite 1.)0-5 deg C; 2.)heated; Yield given. Multistep reaction; | ||
With hydrogenchloride; sodium iodide; sodium nitrite 1.) water, from 0 to 10 deg C, 1 h, 2.) water, RT, overnight; Yield given. Multistep reaction; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With trithiazyl trichloride In tetrachloromethane Ambient temperature; other solvents; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With boron trifluoride diethyl etherate In benzene Heating; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
65% | In toluene for 24h; Heating; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
82% | In toluene for 24h; Heating; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With triethylamine In diethyl ether for 20h; Ambient temperature; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With isopentyl nitrite at 120℃; for 1.5h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With isopentyl nitrite at 120℃; for 1.5h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With isopentyl nitrite at 120℃; for 1.5h; Title compound not separated from byproducts; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
0.11 g | With hydrogenchloride; nickel dichloride; sodium nitrite In hydrogenchloride; water at 0 - 20℃; for 0.833333h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
In toluene at 20℃; for 1h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With sodium acetate; nitrobenzene; copper(II) oxide at 190℃; Behandeln des Reaktionsgemisches mit konz.Schwefelsaeure und Erhitzen des Reaktionsprodukts mit Acetanhydrid in Nitrobenzol auf 155grad und nach Zusatz von konz.Schwefelsaeure auf 90grad; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Stage #1: 2,3,4-trichloroaniline With hydrogenchloride; sodium nitrite Stage #2: potassium cyanide With copper(l) cyanide In water at 20℃; for 0.333333h; | ||
Stage #1: 2,3,4-trichloroaniline With hydrogenchloride; sodium nitrite Stage #2: potassium cyanide |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Stage #1: 2,3,4-trichloroaniline; 2,6-dichloroanisole With isopentyl nitrite at 140℃; Stage #2: With boron tribromide In dichloromethane |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Stage #1: 2,3,4-trichloroaniline; 1,2,4-trichloro-3-methoxybenzene With isopentyl nitrite at 140℃; Stage #2: With boron tribromide In dichloromethane |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 2 steps 1.1: NaNO2; HCl 1.2: CuCN / pH 7 2.1: trimethylaluminum; azidotrimethylsilane / toluene / Heating 2.2: 59 percent / HCl / ethyl acetate; toluene / 0 °C |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 3 steps 1.1: NaNO2; HCl 1.2: CuCN / pH 7 2.1: trimethylaluminum; azidotrimethylsilane / toluene / Heating 2.2: 59 percent / HCl / ethyl acetate; toluene / 0 °C 3.1: triethylamine / acetonitrile / 24 h / 20 °C |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 3 steps 1.1: NaNO2; HCl 1.2: CuCN / pH 7 2.1: trimethylaluminum; azidotrimethylsilane / toluene / Heating 2.2: 59 percent / HCl / ethyl acetate; toluene / 0 °C 3.1: triethylamine / acetonitrile / 24 h / 20 °C |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 3 steps 1: Et3N / diethyl ether / 20 h / Ambient temperature 2: 1 N NaOH / methanol / 3 h / Heating 3: 50 percent / polyphosphoric acid / 3 h / 170 °C |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 2 steps 1: Et3N / diethyl ether / 20 h / Ambient temperature 2: 1 N NaOH / methanol / 3 h / Heating |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 4 steps 1: Et3N / diethyl ether / 20 h / Ambient temperature 2: 1 N NaOH / methanol / 3 h / Heating 3: 50 percent / polyphosphoric acid / 3 h / 170 °C 4: KNO3, TFA / Heating |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 2 steps 1: BF3*Et2O / benzene / Heating 2: benzene / Heating |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 2 steps 1: 1.) concd. hydrochloric acid, sodium nitrite, 2.) sodium iodide / 1.) water, from 0 to 10 deg C, 1 h, 2.) water, RT, overnight 2: 53 percent / tetrahydrofuran / 16 h |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 2 steps 1: 93 percent 2: 62 percent / TiCl4 / CH2Cl2 / Ambient temperature |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With toluene-4-sulfonic acid In chloroform; 1,2-dichloro-ethane at 60℃; for 0.5h; | 3 Reference Example 3; Production of N2-[1,1-dimethyl-2-(methylsulfinyl)ethyl]-N1-(2,3,4-trichlorophenyl)-1,2-benzenedicarboxamide; Phthaloyl dichloride (100.0 g) was added dropwise to a mixture of aqueous sodium hydroxide solution (40.39 g/300 mL), 2-methyl-1-methylthio-2-propanamine (61.66 g) and chloroform (300 mL) at 25°C or lower. After completion of the dropwise addition, the resulting mixture was stirred at 20°C for 30 minutes and the organic layer was separated to prepare a solution of N-[1,1-dimethyl-2-(methylthio)ethyl]isophthalimide in 1,2-dichloroethane. The previously prepared isophthalimide solution was added dropwise to a mixture of 2,3,4-trichloroaniline (91.93 g), p-toluenesulfonic acid monohydrate (2.34 g) and chloroform (75 mL) at 60°C and then stirred for 30 minutes. Subsequently, formic acid (2.27 g) was added thereto and then 35% hydrogen peroxide (52.66 g) was slowly dropped thereinto with heating under reflux. Thereafter, the resulting mixture was stirred at 60°C for 3 hours. An aqueous sodium sulfite solution was added dropwise to the thus obtained reaction mixture at the same temperature to decompose the excess oxidizing agent. Then, the resulting mixture was neutralized with an aqueous sodium hydrogencarbonate solution, after which the organic layer was separated. The organic layer obtained was heated at 60°C. Heptane (800 mL) was added dropwise thereto and the resulting mixture was slowly cooled to 20°C. The crystals precipitated were filtered, washed with water and then dried to obtain 202.44 g (yield 89%) of the title compound. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
66%. | With sodium hydroxide; stannous chloride; sodium nitrite In hydrogenchloride; water | 1.A A. A. 2,3,4-Trichlorophenylhydrazine Fifty grams of 2,3,4-trichloroaniline was added portionwise to a solution of 200 ml of concentrated hydrochloric acid at approximately 0° C. To the reaction mixture was added 17.6 g of sodium nitrite dissolved in 100 ml of water dropwise over 1 hour. Next, 94.8 g of stannous chloride dissolved in 100 ml of concentrated hydrochloric acid was added dropwise to the reaction mixture over a 1 hour period while maintaining the temperature at approximately 0° C. The reaction mixture was stirred for approximately 1 hour at this temperature and then warmed to room temperature and stirred for 20 additional hours. The precipitated solid was collected by filtration and dried. The collected solid was added to a cold solution of 300 ml of 25% aqueous sodium hydroxide and this solution was stirred at approximately 5° C. for 1 hour. This aqueous solution was then extracted with ether and the organic phase was washed with water and saturated sodium chloride, and finally dried over anhydrous magnesium sulfate. The organic phase was evaporated under reduced pressure and the residue was recrystallized from ethanol to afford 35 g of 2,3,4-trichlorophenylhydrazine. Yield 66%. mp=138°-140° C. Analysis was calculated for C6 H6 Cl3 N2 Theory: C, 34.08; H, 2.38; N, 13.25; Found: C, 34.18; H, 2.44; N, 13.29. |
In 2,3,4,6-tetrafluoroaniline | R.1.a REFERENCE EXAMPLE 1 By proceeding in a similar manner but replacing the 2,3,4,6-tetrafluoroaniline by 2,3,4-trichloroaniline there was prepared, after filtration of the insoluble hydrazine hydrochloride, 2,3,4-trichlorophenylhydrazine, m.p. 142°-143° C. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With hydrogenchloride In (2S)-N-methyl-1-phenylpropan-2-amine hydrate; ethanol; water; N,N-dimethyl-formamide | 5 2,4,6-Trichloro-2'-t-butyl-4',6'-dinitrodiphenylamine EXAMPLE 5 2,4,6-Trichloro-2'-t-butyl-4',6'-dinitrodiphenylamine To a solution of 1050 ml of DMF and a 50% oil dispersion of 103.2 g (2.15 moles) of sodium hydride, which was held at -5° under a nitrogen atmosphere, was added 209.4 g (1.066 moles) of 2,4,6-trichloroaniline in 1050 ml of DMF. The trichloroaniline was added in a dropwise manner over a 30-minute period. Then the reaction was stirred for about 45 minutes at a temperature between -5° and 0°. Two hundred and seventy-five grams (1.06 moles) of 2-t-butyl-4,6-dinitrochlorobenzene was added dropwise over a period of 1 hour, while the temperature was maintained between -5° and 0°. The reaction was allowed to warm to room temperature and stirred for about 16 hours. The reaction mixture was poured into about 15 l of an ice-water mixture and then acidified by the addition of hydrochloric acid with stirring. The stirring was continued for about 1 hour, keeping the reaction acidic. The reaction was left in water for about 16 hours. The precipitate that formed was filtered and dried, and then dissolved in 3.5 l of boiling ethanol. After the solution was left standing for about 16 hours, the precipitate was filtered and air dried. A yield of 273.5 g (61.7%) of crystals was obtained, with a melting point of 172°-175°. The identity of the product, 2,4,6-trichloro-2'-t-butyl-4',6'-dinitrodiphenylamine, was confirmed by NMR spectroscopy. Elemental analysis gave the following results: Calculated for C16 H14 N3 O4 Cl3: Theory: C, 45.90; H, 3.37; N, 10.04; Found: C, 46.11; H, 3.44; N, 10.14. The following examples were prepared using the same general procedures detailed above in Examples 1-5. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
In sodium hydroxide; isopropyl alcohol; acetone | 4 EXAMPLE 4 To a stirred solution of 42.0 g ammonium thiocyanate in 200 ml acetone at room temperature was added rapidly from a dropping funnel 70.3 g benzoyl chloride. The mixture was refluxed for five minutes and then a solution of 98.3 g 2,3,4-trichloroaniline in 150 ml acetone was added gradually so as to maintain gentle reflux. A thick precipitate formed and it was necessary to add more acetone to facilitate stirring. The mixture was stirred and refluxed for thirty minutes and then poured into iced water. The benzoyl derivative was filtered off, washed with water, then suspended in 1 liter of 10 percent sodium hydroxide solution. The mixture was stirred and heated on the steambath for one hour, treated with charcoal and filtered whilst hot. It was acidified with concentrated hydrochloric acid and then made just alkaline with ammonium hydroxide solution. The solid was filtered off, dried and recrystallized with charcoal from propan-2-ol to give 2,3,4-trichlorophenylthiourea, melting point 185°-186° C. The following novel compound was made by a similar method, 2-(4-chloro-2-ethylphenylimino)imidazolidine, melting point 115°-117° C. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With ammonium hydroxide; sodium nitrite In hydrogenchloride; sulfuric acid; acetic acid | R.1.c REFERENCE EXAMPLE 1 (c) 2,3,4-Trichloroaniline (100 g) was dissolved with stirring in glacial acetic acid (875 ml) at 55°-60° C. A solution of sodium nitrite (39.5 g) in concentrated sulphuric acid (300 ml) was then added over 15 minutes at 55°-60° C. to the solution thus obtained. The viscous mixture obtained was cooled to 5°-10° C. and a solution of stannous chloride dihydrate (437 g) in concentrated hydrochloric acid (375 ml) was added at 5°-10° C. over 20 minutes. A fine, off-white solid precipitated. To aid filtration, the mixture was warmed to 60° C., allowed to cool to laboratory temperature and then filtered. The precipitate was washed on the filter with saturated aqueous sodium chloride solution (100 ml). The damp powder thus obtained was added to a stirred mixture of aqueous ammonia (1.3 liters; S.G. 0.880) and ice. The fine slurry which formed was filtered and the precipitate obtained was dried at 80° C., and boiled twice with chloroform (2*1.5 liters). The chloroform extracts were combined and evaporated to dryness to give 2,3,4-trichlorophenylhydrazine (86 g), m.p. 142°-143° C., in the form of a colourless powder. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With 2-Methyl-2-nitropropane; copper(ll) bromide In acetonitrile at 60℃; for 0.5h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With sodium hydrogencarbonate In dichloromethane; water; toluene at 0 - 20℃; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With potassium <i>tert</i>-butylate In 1,4-dioxane at 120℃; for 14h; Inert atmosphere; | 77.77A EXAMPLE 77 5-{ [2-methoxy-4-( iperazin-l -yI)phenyl]amino}-7-[(2,3,4-trichlorophenyI)amino]pyrido[3,4- d]pyridazin-4(3H)-one EXAMPLE 77A tert-butyl4-(3-methoxy-4-(4-oxo-7-(2,3,4-trichlorophenylamino)-3,4-dihydropyrido[3,4- +). |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
With sodium hydroxide In N,N-dimethyl-formamide at 20℃; for 5h; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
In ethanol for 8h; Reflux; | 3.11 6.3.2 Ethyl 4-(2′,4′-dibromophenylamino)cyclohex-3-en-6-methyl-2-oxo-1-oate (21) General procedure: To a solution of ethyl 4-hydroxy-6-methyl-2-oxocyclohex-3-en-1-oate (1g, 5mmol) in 80mL of absolute ethanol was added a solution of 2,4-dibromoaniline (98%, 1.28g, 5mmol) in 50mL of absolute ethanol and the reaction mixture refluxed with stirring for 8h. The reaction mixture was evaporated using rotary evaporator, and the residue recrystallized from ethyl acetate/petroleum ether bp 60-80°C to obtain 0.60g of enaminone 21, 28% yield. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
78% | Stage #1: 2,3,4-trichloroaniline With sodium hydride In tetrahydrofuran at 20℃; for 0.5h; Stage #2: 2,6-dichloro-3,5-dinitrotoluene In tetrahydrofuran for 5.5h; | 22 4.2.1. General procedure for the synthesis of compounds P1-21, P25-P28 and P33 General procedure: Substituted/unsubstituted aniline 6 (1equiv) was added in portions to a suspension of NaH (60%, 2 equiv) and tetrahydrofuran (THF) at room temperature, the mixture was stirred for 30 min. 2,6-Dichloro-3,5-dinitrotulune (3, 1.2equiv) in THF was added within 30 min, then stirred for another 5 h. After the reaction was over by thin-layer chromatography (TLC) monitoring, the reaction mixture was filtered. The filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (ethyl acetate/petroleum ether=1:20) to give the target compounds. 4.2.1.22 3-Chloro-2-methyl-4,6-dinitro-N-(2,3,4-trichlorophenyl)aniline (P25) Brown solid; mp 122-123 °C; yield 78%. 1H NMR (300 MHz, CDCl3): δ 8.84 (s, 1H, NH), 8.65 (s, 1H, Ph-5'-H), 7.28 (d, 1H, Ph-5-H, J = 8.7 Hz), 6.42 (d, 1H, Ph-6-H, J = 8.7 Hz), 2.17 (s, 3H, Ph-2'-CH3). Anal. Calcd for C13H7Cl4N3O4: C, 37.99; H, 1.72; N, 10.22. Found: C, 37.97; H, 1.78; N, 10.26. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
89% | In N,N-dimethyl-formamide; for 24h;Reflux; | General procedure: A mixture of 4-isothiocyanato benzenesulfonamide 2 (2.14 g, 0.01 mol) and an appropriate amine (0.012 mol) in dry dimethylformamide (15 mL) containing trimethylamine (0.3 mL) was refluxed for 24 h., then left to cool. The solid product formed upon pouring onto ice/water was collected by filtration and recrystallized from ethanol-dimethylformamide to give 3-16, respectively. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
97% | With chloro[(di(1-adamantyl)-N-butylphosphine)-2-(2-aminobiphenyl)]palladium(II); potassium carbonate In N,N-dimethyl-formamide at 50℃; Inert atmosphere; | 6 2,3-dichloro-4-amino-biphenyl Under nitrogen, 1L four-mouth bottle, mechanical stirring, adding 500mLN, N-dimethyl formamide, 77g2, 3, 4-trichloroaniline, 47.8g phenyltheophylline boric acid, 108g potassium carbonate, 0.26g palladium catalyst 2GAd2 (n-bu) PPd (Chloro [(di (1-adamantyl)-N-butylphosphine) - 2 - (2-aminobiphenyl)] palladium (II)), in 50 °C reaction sleepovers. Plus 20g naoh 100 ml aqueous solution quenching, 300 ml ethyl acetate extraction, the organic phase exsolution, to obtain crystal micro purple 2,3-dichloro-4-aminobiphenyl 91g, yield 97%. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
97% | With chloro[(di(1-adamantyl)-N-butylphosphine)-2-(2-aminobiphenyl)]palladium(II); potassium carbonate In N,N-dimethyl-formamide at 50℃; Inert atmosphere; | 7 3-chloro -2,4-diphenyl-aniline preparation Under nitrogen, 1L four-mouth bottle, mechanical stirring, adding 500mLN, N-dimethyl formamide, 77g2, 3, 4-trichloroaniline, 95.6g phenyltheophylline boric acid, 220g potassium carbonate, 0.26g palladium catalyst 2GAd2 (n-bu) PPd (Chloro [(di (1-adamantyl)-N-butylphosphine) - 2 - (2-aminobiphenyl)] palladium (II)), in 50 °C reaction sleepovers. Plus 20g naoh 100 ml aqueous solution quenching, 300 ml ethyl acetate extraction, the organic phase exsolution, to obtain crystal micro purple 3-chloro -2,4- diphenyl aniline 107g, the yield is 97% |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
97% | With chloro[(di(1-adamantyl)-N-butylphosphine)-2-(2-aminobiphenyl)]palladium(II); potassium carbonate In N,N-dimethyl-formamide at 100℃; Inert atmosphere; | 8 2, 3, 4-triphenylporphyrin aniline preparation Under nitrogen, 1L four-mouth bottle, mechanical stirring, adding 500mLN, N-dimethyl formamide, 77g2, 3, 4-trichloroaniline, 153g phenyltheophylline boric acid, 346g potassium carbonate, 0.26g palladium catalyst 2GAd2 (n-bu) PPd (Chloro [(di (1-adamantyl)-N-butylphosphine) - 2 - (2-aminobiphenyl)] palladium (II)), in the 100 °C reaction sleepovers. Plus 20g naoh 100 ml aqueous solution quenching, 300 ml ethyl acetate extraction, the organic phase exsolution, to obtain white solid 2, 3, 4- triphenyl aniline 122g, yield 97%. |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 2 steps 1.1: sodium nitrite; hydrogenchloride / water / 1 h / -5 - 5 °C 1.2: 1 h / 50 - 80 °C 2.1: nitric acid; sulfuric acid / 1,2-dichloro-ethane / 10 h / 0 - 50 °C |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
46% | With potassium carbonate; potassium iodide In N,N-dimethyl-formamide at 115℃; for 24h; Inert atmosphere; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 3 steps 1.1: hydrogenchloride / lithium hydroxide monohydrate; acetonitrile / 1 h / 20 °C 1.2: 1 h / 0 °C / Inert atmosphere 2.1: Cupric sulfate; sodium ascorbate powder / methanol; <i>tert</i>-butyl alcohol; lithium hydroxide monohydrate / 16 h / 40 °C 3.1: methanol; anhydrous sodium carbonate / methanol / 16 h / 20 °C / Inert atmosphere |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Stage #1: 2,3,4-trichloroaniline With hydrogenchloride In lithium hydroxide monohydrate; acetonitrile at 20℃; for 1h; Stage #2: With Caswell No. 744A In lithium hydroxide monohydrate; acetonitrile at 0℃; for 1h; Inert atmosphere; |
Yield | Reaction Conditions | Operation in experiment |
---|---|---|
Multi-step reaction with 2 steps 1.1: hydrogenchloride / lithium hydroxide monohydrate; acetonitrile / 1 h / 20 °C 1.2: 1 h / 0 °C / Inert atmosphere 2.1: Cupric sulfate; sodium ascorbate powder / methanol; <i>tert</i>-butyl alcohol; lithium hydroxide monohydrate / 16 h / 40 °C |
Tags: 634-67-3 synthesis path| 634-67-3 SDS| 634-67-3 COA| 634-67-3 purity| 634-67-3 application| 634-67-3 NMR| 634-67-3 COA| 634-67-3 structure
[ 41946-53-6 ]
1,4-Diamino-2,3-dichlorobenzene
Similarity: 0.96
[ 41946-53-6 ]
1,4-Diamino-2,3-dichlorobenzene
Similarity: 0.96
[ 41946-53-6 ]
1,4-Diamino-2,3-dichlorobenzene
Similarity: 0.96
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P280 | Wear protective gloves/protective clothing/eye protection/face protection. |
P281 | Use personal protective equipment as required. |
P282 | Wear cold insulating gloves/face shield/eye protection. |
P283 | Wear fire/flame resistant/retardant clothing. |
P284 | Wear respiratory protection. |
P285 | In case of inadequate ventilation wear respiratory protection. |
P231 + P232 | Handle under inert gas. Protect from moisture. |
P235 + P410 | Keep cool. Protect from sunlight. |
Response | |
Code | Phrase |
P301 | IF SWALLOWED: |
P304 | IF INHALED: |
P305 | IF IN EYES: |
P306 | IF ON CLOTHING: |
P307 | IF exposed: |
P308 | IF exposed or concerned: |
P309 | IF exposed or if you feel unwell: |
P310 | Immediately call a POISON CENTER or doctor/physician. |
P311 | Call a POISON CENTER or doctor/physician. |
P312 | Call a POISON CENTER or doctor/physician if you feel unwell. |
P313 | Get medical advice/attention. |
P314 | Get medical advice/attention if you feel unwell. |
P315 | Get immediate medical advice/attention. |
P320 | |
P302 + P352 | IF ON SKIN: wash with plenty of soap and water. |
P321 | |
P322 | |
P330 | Rinse mouth. |
P331 | Do NOT induce vomiting. |
P332 | IF SKIN irritation occurs: |
P333 | If skin irritation or rash occurs: |
P334 | Immerse in cool water/wrap n wet bandages. |
P335 | Brush off loose particles from skin. |
P336 | Thaw frosted parts with lukewarm water. Do not rub affected area. |
P337 | If eye irritation persists: |
P338 | Remove contact lenses, if present and easy to do. Continue rinsing. |
P340 | Remove victim to fresh air and keep at rest in a position comfortable for breathing. |
P341 | If breathing is difficult, remove victim to fresh air and keep at rest in a position comfortable for breathing. |
P342 | If experiencing respiratory symptoms: |
P350 | Gently wash with plenty of soap and water. |
P351 | Rinse cautiously with water for several minutes. |
P352 | Wash with plenty of soap and water. |
P353 | Rinse skin with water/shower. |
P360 | Rinse immediately contaminated clothing and skin with plenty of water before removing clothes. |
P361 | Remove/Take off immediately all contaminated clothing. |
P362 | Take off contaminated clothing and wash before reuse. |
P363 | Wash contaminated clothing before reuse. |
P370 | In case of fire: |
P371 | In case of major fire and large quantities: |
P372 | Explosion risk in case of fire. |
P373 | DO NOT fight fire when fire reaches explosives. |
P374 | Fight fire with normal precautions from a reasonable distance. |
P376 | Stop leak if safe to do so. Oxidising gases (section 2.4) 1 |
P377 | Leaking gas fire: Do not extinguish, unless leak can be stopped safely. |
P378 | |
P380 | Evacuate area. |
P381 | Eliminate all ignition sources if safe to do so. |
P390 | Absorb spillage to prevent material damage. |
P391 | Collect spillage. Hazardous to the aquatic environment |
P301 + P310 | IF SWALLOWED: Immediately call a POISON CENTER or doctor/physician. |
P301 + P312 | IF SWALLOWED: call a POISON CENTER or doctor/physician IF you feel unwell. |
P301 + P330 + P331 | IF SWALLOWED: Rinse mouth. Do NOT induce vomiting. |
P302 + P334 | IF ON SKIN: Immerse in cool water/wrap in wet bandages. |
P302 + P350 | IF ON SKIN: Gently wash with plenty of soap and water. |
P303 + P361 + P353 | IF ON SKIN (or hair): Remove/Take off Immediately all contaminated clothing. Rinse SKIN with water/shower. |
P304 + P312 | IF INHALED: Call a POISON CENTER or doctor/physician if you feel unwell. |
P304 + P340 | IF INHALED: Remove victim to fresh air and Keep at rest in a position comfortable for breathing. |
P304 + P341 | IF INHALED: If breathing is difficult, remove victim to fresh air and keep at rest in a position comfortable for breathing. |
P305 + P351 + P338 | IF IN EYES: Rinse cautiously with water for several minutes. Remove contact lenses, if present and easy to do. Continue rinsing. |
P306 + P360 | IF ON CLOTHING: Rinse Immediately contaminated CLOTHING and SKIN with plenty of water before removing clothes. |
P307 + P311 | IF exposed: call a POISON CENTER or doctor/physician. |
P308 + P313 | IF exposed or concerned: Get medical advice/attention. |
P309 + P311 | IF exposed or if you feel unwell: call a POISON CENTER or doctor/physician. |
P332 + P313 | IF SKIN irritation occurs: Get medical advice/attention. |
P333 + P313 | IF SKIN irritation or rash occurs: Get medical advice/attention. |
P335 + P334 | Brush off loose particles from skin. Immerse in cool water/wrap in wet bandages. |
P337 + P313 | IF eye irritation persists: Get medical advice/attention. |
P342 + P311 | IF experiencing respiratory symptoms: call a POISON CENTER or doctor/physician. |
P370 + P376 | In case of fire: Stop leak if safe to Do so. |
P370 + P378 | In case of fire: |
P370 + P380 | In case of fire: Evacuate area. |
P370 + P380 + P375 | In case of fire: Evacuate area. Fight fire remotely due to the risk of explosion. |
P371 + P380 + P375 | In case of major fire and large quantities: Evacuate area. Fight fire remotely due to the risk of explosion. |
Storage | |
Code | Phrase |
P401 | |
P402 | Store in a dry place. |
P403 | Store in a well-ventilated place. |
P404 | Store in a closed container. |
P405 | Store locked up. |
P406 | Store in corrosive resistant/ container with a resistant inner liner. |
P407 | Maintain air gap between stacks/pallets. |
P410 | Protect from sunlight. |
P411 | |
P412 | Do not expose to temperatures exceeding 50 oC/ 122 oF. |
P413 | |
P420 | Store away from other materials. |
P422 | |
P402 + P404 | Store in a dry place. Store in a closed container. |
P403 + P233 | Store in a well-ventilated place. Keep container tightly closed. |
P403 + P235 | Store in a well-ventilated place. Keep cool. |
P410 + P403 | Protect from sunlight. Store in a well-ventilated place. |
P410 + P412 | Protect from sunlight. Do not expose to temperatures exceeding 50 oC/122oF. |
P411 + P235 | Keep cool. |
Disposal | |
Code | Phrase |
P501 | Dispose of contents/container to ... |
P502 | Refer to manufacturer/supplier for information on recovery/recycling |
Physical hazards | |
Code | Phrase |
H200 | Unstable explosive |
H201 | Explosive; mass explosion hazard |
H202 | Explosive; severe projection hazard |
H203 | Explosive; fire, blast or projection hazard |
H204 | Fire or projection hazard |
H205 | May mass explode in fire |
H220 | Extremely flammable gas |
H221 | Flammable gas |
H222 | Extremely flammable aerosol |
H223 | Flammable aerosol |
H224 | Extremely flammable liquid and vapour |
H225 | Highly flammable liquid and vapour |
H226 | Flammable liquid and vapour |
H227 | Combustible liquid |
H228 | Flammable solid |
H229 | Pressurized container: may burst if heated |
H230 | May react explosively even in the absence of air |
H231 | May react explosively even in the absence of air at elevated pressure and/or temperature |
H240 | Heating may cause an explosion |
H241 | Heating may cause a fire or explosion |
H242 | Heating may cause a fire |
H250 | Catches fire spontaneously if exposed to air |
H251 | Self-heating; may catch fire |
H252 | Self-heating in large quantities; may catch fire |
H260 | In contact with water releases flammable gases which may ignite spontaneously |
H261 | In contact with water releases flammable gas |
H270 | May cause or intensify fire; oxidizer |
H271 | May cause fire or explosion; strong oxidizer |
H272 | May intensify fire; oxidizer |
H280 | Contains gas under pressure; may explode if heated |
H281 | Contains refrigerated gas; may cause cryogenic burns or injury |
H290 | May be corrosive to metals |
Health hazards | |
Code | Phrase |
H300 | Fatal if swallowed |
H301 | Toxic if swallowed |
H302 | Harmful if swallowed |
H303 | May be harmful if swallowed |
H304 | May be fatal if swallowed and enters airways |
H305 | May be harmful if swallowed and enters airways |
H310 | Fatal in contact with skin |
H311 | Toxic in contact with skin |
H312 | Harmful in contact with skin |
H313 | May be harmful in contact with skin |
H314 | Causes severe skin burns and eye damage |
H315 | Causes skin irritation |
H316 | Causes mild skin irritation |
H317 | May cause an allergic skin reaction |
H318 | Causes serious eye damage |
H319 | Causes serious eye irritation |
H320 | Causes eye irritation |
H330 | Fatal if inhaled |
H331 | Toxic if inhaled |
H332 | Harmful if inhaled |
H333 | May be harmful if inhaled |
H334 | May cause allergy or asthma symptoms or breathing difficulties if inhaled |
H335 | May cause respiratory irritation |
H336 | May cause drowsiness or dizziness |
H340 | May cause genetic defects |
H341 | Suspected of causing genetic defects |
H350 | May cause cancer |
H351 | Suspected of causing cancer |
H360 | May damage fertility or the unborn child |
H361 | Suspected of damaging fertility or the unborn child |
H361d | Suspected of damaging the unborn child |
H362 | May cause harm to breast-fed children |
H370 | Causes damage to organs |
H371 | May cause damage to organs |
H372 | Causes damage to organs through prolonged or repeated exposure |
H373 | May cause damage to organs through prolonged or repeated exposure |
Environmental hazards | |
Code | Phrase |
H400 | Very toxic to aquatic life |
H401 | Toxic to aquatic life |
H402 | Harmful to aquatic life |
H410 | Very toxic to aquatic life with long-lasting effects |
H411 | Toxic to aquatic life with long-lasting effects |
H412 | Harmful to aquatic life with long-lasting effects |
H413 | May cause long-lasting harmful effects to aquatic life |
H420 | Harms public health and the environment by destroying ozone in the upper atmosphere |
Sorry,this product has been discontinued.
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