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[ CAS No. 219581-07-4 ] {[proInfo.proName]}

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Chemical Structure| 219581-07-4
Chemical Structure| 219581-07-4
Structure of 219581-07-4 * Storage: {[proInfo.prStorage]}
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Product Details of [ 219581-07-4 ]

CAS No. :219581-07-4 MDL No. :MFCD00236301
Formula : C7H4F4O Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 180.10 Pubchem ID :-
Synonyms :

Safety of [ 219581-07-4 ]

Signal Word:Danger Class:6.1,8
Precautionary Statements:P260-P280-P301+P310-P304+P340 UN#:2927
Hazard Statements:H301+H331-H314-H317-H411 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 219581-07-4 ]

* 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.

  • Downstream synthetic route of [ 219581-07-4 ]

[ 219581-07-4 ] Synthesis Path-Downstream   1~9

  • 1
  • [ 445303-67-3 ]
  • [ 219581-07-4 ]
YieldReaction ConditionsOperation in experiment
With Oxone In water; acetone for 0.25h; 7 A solution of OXONE (1 .50 g, 2.45 mmol) in water (7.8 mL) was added drop-wise over approximately 4 minutes to a solution of 2-[3-fluoro-4-(trifluoromethyl)phenyl]-4,4,5,5- tetramethyl-1 ,3,2-dioxaborolane (710 mg, 2.4 mmol) in acetone (7.8 mL). A precipitate formed during addition of the OXONE. The reaction mixture was stirred vigorously for 15 minutes then quenched with 10% w/v aqueous solution of sodium metabisulfite (20 mL). The aqueous layer was extracted with dichloromethane (x 3), dried over anhydrous sodium sulfate, filtered, and concentrated in vacuo to afford the title compound as a light yellow oil which was used without purification in the next step.LCMS Rt = 1 .65 min MS m/z 179 [MH]-
  • 2
  • [ 219581-07-4 ]
  • [ 1354818-79-3 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1: iodine; silver trifluoroacetate / chloroform / 1 h 2: cesium fluoride; copper(l) iodide / tetrakis(triphenylphosphine) palladium(0) / N,N-dimethyl-formamide / 1.5 h / 45 °C / Inert atmosphere 3: potassium carbonate / dimethyl sulfoxide / 24 h / 75 °C
  • 3
  • [ 219581-07-4 ]
  • [ 1354819-06-9 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 4 steps 1: iodine; silver trifluoroacetate / chloroform / 1 h 2: cesium fluoride; copper(l) iodide / tetrakis(triphenylphosphine) palladium(0) / N,N-dimethyl-formamide / 1.5 h / 45 °C / Inert atmosphere 3: potassium carbonate / dimethyl sulfoxide / 24 h / 75 °C 4: acetone / 0.25 h / 20 °C
  • 4
  • [ 219581-07-4 ]
  • [ 1235407-47-2 ]
YieldReaction ConditionsOperation in experiment
With iodine; silver trifluoroacetate In chloroform for 1h; 8 A solution of iodine (0.874 g, 3.44 mmol) in chloroform (17.1 mL) was added in a drop- wise manner over 1 .5 hours to a mixture of 3-fluoro-4-(trifluoromethyl)phenol (Preparation 7, 620 mg, 3.4 mmol) and silver trifluoroacetate (0.760 g, 3.44 mmol) in chloroform (3.4 ml_). On completion of the addition, the reaction mixture was stirred for 1 hour. The reaction mixture was then filtered through diatomaceous earth, and the filtrate washed successively with 10% w/v aqueous sodium thiosulfate, half-saturated aqueous sodium bicarbonate, water and brine. The organic phase was dried over anhydrous sodium sulfate, filtered, and concentrated onto diatomaceous earth . The residue was purified by automated silica gel flash chromatography (100% hexanes to 50% dichloromethane in hexanes gradient elution) and concentrated in vacuo to afford the title compound as a light yellow oil (579 mg).1 HNMR (de-DMSO): δ 6.85 (d, 1 H), 7.97 (d, 1 H), 1 1 .81 (s, 1 H).LCMS Rt = 1 .79 min MS m/z 305 [MH]-
With N-iodo-succinimide; sulfuric acid; acetic acid 5-fluoro-2-iodo-4-(trifluoromethyl)phenol The requisite 5-fluoro-2-iodo-4-(trifluoromethyl)phenol was synthesized via treatment of a solution of 3-fluoro-4-(trifluoromethyl)phenol in acetic acid with N-iodosuccinimide and sulfuric acid.
  • 5
  • [ 219581-07-4 ]
  • [ 1235407-46-1 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: iodine; silver trifluoroacetate / chloroform / 1 h 2: cesium fluoride; copper(l) iodide / tetrakis(triphenylphosphine) palladium(0) / N,N-dimethyl-formamide / 1.5 h / 45 °C / Inert atmosphere
  • 6
  • [ 5292-43-3 ]
  • [ 219581-07-4 ]
  • 2-(3-fluoro-4-(trifluoromethyl)phenoxy)acetic acid [ No CAS ]
YieldReaction ConditionsOperation in experiment
1.18 g Stage #1: bromoacetic acid <i>tert</i>-butyl ester; 3-fluoro-4-(trifluoromethyl)phenol With potassium carbonate In N,N-dimethyl-formamide at 65℃; for 16h; Stage #2: With water; sodium hydroxide In methanol at 20℃; 574.574A Example 574A: 2-(3-fluoro-4-(trifluoromethyl)phenoxy)acetic acid To a solution of 3-fluoro-4-(trifluoromethyl)phenol (0.9 g, 5.00 mmol) in N,N- dimethylformamide (10.0 mL) at ambient temperature was added potassium carbonate (1.381 g, 9.99 mmol) and teri-butyl bromoacetate (0.843 mL, 5.75 mmol). This mixture was stirred at 65 °C for 16 hours, allowed to cool to ambient temperature and was diluted with ethyl acetate (50 mL) and 0 (50 mL). The layers were separated, and the aqueous layer was extracted with ethyl acetate (3 x 15 mL). The combined organic layers were dried over anhydrous Na2SO/t, filtered, and concentrated under reduced pressure to give the ester (1.18 g, 4.96 mmol, 99 % yield). This ester was dissolved in methanol/water (3 : 1 , 20 mL) and treated with 12.5 N NaOH aqueous solution (4.00 mL, 50.0 mmol). The mixture was stirred at ambient temperature overnight. The mixture was concentrated, and the residue was acidified with 1 N aqueous HC1. The precipitate was collected by filtration and air-dried to give 1.18 g of the title compound.JH NMR (400 MHz, DMSO-
  • 7
  • [ 219581-07-4 ]
  • (S)-N-(4-amino-3-hydroxybicyclo[2.2.2]octan-1-yl)-2-(3-fluoro-4-(trifluoromethyl)phenoxy)acetamide trifluoroacetic acid [ No CAS ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1.1: potassium carbonate / N,N-dimethyl-formamide / 16 h / 65 °C 1.2: 20 °C 2.1: N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate / N,N-dimethyl-formamide / 16 h / 20 °C 2.2: 1 h 2.3: 0.75 h
  • 8
  • [ 219581-07-4 ]
  • (S)-2-((2,2-difluorobenzo[d][1,3]dioxol-5-yl)oxy)-N-(4-(2-(3-fluoro-4-(trifluoromethyl)phenoxy)acetamido)-2-hydroxybicyclo[2.2.2 ]octan-1-yl)acetamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1.1: potassium carbonate / N,N-dimethyl-formamide / 16 h / 65 °C 1.2: 20 °C 2.1: N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate / N,N-dimethyl-formamide / 16 h / 20 °C 2.2: 1 h 2.3: 0.75 h 3.1: N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate / N,N-dimethyl-formamide / 2 h / 20 °C
  • 9
  • [ 219581-07-4 ]
  • N,N'-[(2S)-2-hydroxybicyclo[2.2.2]octane-1,4-diyl]bis{2-[3-fluoro-4-(trifluoromethyl)phenoxy]acetamide} [ No CAS ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1.1: potassium carbonate / N,N-dimethyl-formamide / 16 h / 65 °C 1.2: 20 °C 2.1: N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate / N,N-dimethyl-formamide / 1 h / 20 °C
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