[ CAS No. 1824239-57-7 ] {[proInfo.proName]}

Name: 1824239-57-7|tert-Butyl (3-iodocyclobutyl)carbamate|97%
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Quality Control of [ 1824239-57-7 ]

COA NMR CNMR HPLC LC-MS

Related Doc. of [ 1824239-57-7 ]

SDS Specification

Alternatived Products of [ 1824239-57-7 ]

Product Details of [ 1824239-57-7 ]

CAS No. :	1824239-57-7	MDL No. :	MFCD24530658
Formula :	C₉H₁₆INO₂	Boiling Point :	-
Linear Structure Formula :	-	InChI Key :	XGEFFDGFPRWHAW-UHFFFAOYSA-N
M.W :	297.13	Pubchem ID :	72207528
Synonyms :

Calculated chemistry of [ 1824239-57-7 ] Expand+

Physicochemical Properties

Num. heavy atoms :	13
Num. arom. heavy atoms :	0
Fraction Csp3 :	0.89
Num. rotatable bonds :	4
Num. H-bond acceptors :	2.0
Num. H-bond donors :	1.0
Molar Refractivity :	60.74
TPSA :	38.33 Å²

Pharmacokinetics

GI absorption :	High
BBB permeant :	Yes
P-gp substrate :	No
CYP1A2 inhibitor :	No
CYP2C19 inhibitor :	No
CYP2C9 inhibitor :	No
CYP2D6 inhibitor :	No
CYP3A4 inhibitor :	No
Log Kp (skin permeation) :	-6.34 cm/s

Lipophilicity

Log Po/w (iLOGP) :	2.77
Log Po/w (XLOGP3) :	2.49
Log Po/w (WLOGP) :	2.48
Log Po/w (MLOGP) :	2.01
Log Po/w (SILICOS-IT) :	1.75
Consensus Log Po/w :	2.3

Druglikeness

Lipinski :	0.0
Ghose :	None
Veber :	0.0
Egan :	0.0
Muegge :	0.0
Bioavailability Score :	0.55

Water Solubility

Log S (ESOL) :	-2.99
Solubility :	0.306 mg/ml ; 0.00103 mol/l
Class :	Soluble
Log S (Ali) :	-2.94
Solubility :	0.341 mg/ml ; 0.00115 mol/l
Class :	Soluble
Log S (SILICOS-IT) :	-2.42
Solubility :	1.13 mg/ml ; 0.0038 mol/l
Class :	Soluble

Medicinal Chemistry

PAINS :	0.0 alert
Brenk :	2.0 alert
Leadlikeness :	0.0
Synthetic accessibility :	3.22

Safety of [ 1824239-57-7 ]

Signal Word:	Warning	Class:	N/A
Precautionary Statements:	P280-P305+P351+P338	UN#:	N/A
Hazard Statements:	H302	Packing Group:	N/A
GHS Pictogram:

Application In Synthesis of [ 1824239-57-7 ]

* 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 [ 1824239-57-7 ]

[ 1824239-57-7 ] Synthesis Path-Downstream 1~13

1
[ 1824239-57-7 ]
[ 2416026-59-8 ]
[ 2416026-60-1 ]

Yield	Reaction Conditions	Operation in experiment
	With (1,2-dimethoxyethane)dichloronickel(II); tris-(trimethylsilyl)silane; [4,4′-bis(1,1-dimethylethyl)-2,2′-bipyridine-N1,N1′]bis{3,5-difluoro-2-[5-(trifluoromethyl)-2-pyridinyl-κN]phenyl-κC}iridium(III) hexafluorophosphate; sodium carbonate; 4,4'-di-tert-butyl-2,2'-bipyridine In 1,4-dioxane for 17h; Inert atmosphere; UV-irradiation;	6-7.3 Step 3 : tert-Butyl 3 -bromo-5-methyl-6-(8-methyl-[ 1 ,2,4]triazolo[ 1 ,5-a]pyridin-6-yl)- 1H- indazole-l-carboxylate (100 mg, 0.226 mmol), tert-butyl (3-iodocyclobutyl)carbamate (0464) (134 mg, 0.452 mmol), tris(trimethyl)silane (56.6 pL, 0.339 mmol), Ir(dF(CF3)ppy) (0465) 2(dtbbpy)PF6 (2.54 mg, 2.261 pmol), and Na2C03 (96 mg, 0.904 mmol) were placed in a (0466) Teflon screw cap vial with a stir bar. l,4-Dioxane (1884 pL) was added and the suspension was degassed (cap off) with nitrogen for 5 minutes. To a separate vial was added nickel(II) chloride ethylene glycol dimethyl ether complex (2.484 mg, 0.011 mmol) and 4,4'-di-tert-butyl-2,2'-bipyridine (3.64 mg, 0.014 mmol), which was evacuated and backfilled with nitrogen followed by l,4-dioxane (377 pL). This solution was degassed (0467) (cap on) with nitrogen gas for 10 minutes and stirred. The resulting solution was added to the reaction mixture, which was further degassed with nitrogen gas for another 10 minutes (cap on). The resulting suspension was placed in a block with stirring and blue (0468) Kessil lamp irradiation. After stirring overnight (17 hours) in front of 2 Kessil lamps, the reaction mixture was diluted with DCM and then dried with MgS04. The mixture was filtered, concentrated and purified on silica (12 g silica gel, hexanes/EtOAc; 0-100% EtOAc over 12 min.) to afford tert-butyl 3-(3-((tert-butoxycarbonyl)amino)cyclobutyl)-5- methyl-6-(8-methyl-[ 1 ,2,4]triazolo[ 1 ,5 -a]pyridin-6-yl)- lH-indazole- 1 -carboxylate (37 mg, 0.069 mmol, 30.7 % yield) mixed with de-iodinated azetidine starting material in a 3: 1 ratio favoring the desired product, carried forward as mixture. MS (M+1) m/z: 533 (MH+). LC retention time 1.04 min [Al]

Reference： [1]Current Patent Assignee: BRISTOL-MYERS SQUIBB CO - WO2020/86503, 2020, A1 Location in patent: Page/Page column 63-64

2
[ 1824239-57-7 ]
[ 2448524-11-4 ]
[ CAS Unavailable ]

Yield	Reaction Conditions	Operation in experiment
	Stage #1: tert-butyl N-(3-iodocyclobutyl)carbamate With zinc In N,N-dimethyl acetamide at 65℃; for 0.333333h; Stage #2: (18aS)-13-chloro-2-fluoro-11-methyl-8,9,10,11,19,20,21,22-octahydro-18aH,24H-18,15-(metheno)pyrido[2,1-l]pyrimido[6,1-h][1,4,7,9,10,13]benzoxapentaazacyclohexadecine-7,24(6H)-dione With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; copper(l) iodide In N,N-dimethyl acetamide at 85℃; for 0.0833333h;	(18aS)-13-(Azetidin-3-yl)-2-fluoro-11-methyl-8,9,10,11,19,20,21,22-octahydro-18aH,24H-18,15-(metheno)pyrido[2,1-l]pyrimido[6,1-h][1,4,7,9,10,13]benzoxapentaazacyclohexadecine-7,24(6H)-dione (48) General procedure: To a solution of 1-Boc-3-iodoazetidine (0.25 g, 0.883 mmol, 5.0 eq) in N,N-dimethylacetamide (2.0 mL) was added zinc powder (59 mg, 0.901 mmol, 5.1 eq) at 65 °C. After stirring for 20 min, a solution of 41c (86 mg, 0.177 mmol) in N,N-dimethylacetamide (2.0 mL) was placed in another flask, and copper iodide (I) (6.7 mg, 0.035 mmol, 0.20 eq) and [1,1'-bis(diphenylphosphino)ferrocene]dichloropalladium (II) (78 mg, 0.106 mmol, 0.60 eq) were added. After stirring at 85 °C for 5 min, the reaction mixture was added to the prepared zinc reagent. After stirring at 85 °C for 5 min, the reaction mixture was poured into saturated aqueous ammonium chloride and extracted with ethyl acetate. The organic layer was washed with brine and dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The residue was purified using silica gel column chromatography (NH 50%-100% ethyl acetate in hexane) to obtain tert-butyl 3-[(18aS)-2-fluoro-11-methyl-7,24-dioxo-6,7,8,9,10,11,19,20,21,22-decahydro-18aH,24H-18,15-(metheno)pyrido[2,1-l]pyrimido[6,1-h][1,4,7,9,10,13]benzoxapentaazacyclohexadecin-13-yl]azetidine-1-carboxylate (79 mg, 0.130 mmol, 73%) as a pale brown amorphous substance. To a solution of tert-butyl 3-[(18aS)-2-fluoro-11-methyl-7,24-dioxo-6,7,8,9,10,11,19,20,21,22-decahydro-18aH,24H-18,15-(metheno)pyrido[2,1-l]pyrimido[6,1-h][1,4,7,9,10,13]benzoxapentaazacyclohexadecin-13-yl]azetidine-1-carboxylate (78 mg, 0.128 mmol) in chloroform (1.0 mL) was added trifluoroacetic acid (1.0 mL). After stirring at room temperature for 1 h, the reaction mixture was poured into saturated aqueous sodium bicarbonate and extracted with chloroform. The organic layer was dried through a phase separator and concentrated under reduced pressure. The residue was purified using reversed-phase preparative HPLC to obtain 48 (27 mg, 0.054 mmol, 42%) as a colorless powder. 1H NMR (400 MHz, CDCl3) δ ppm 1.19-1.72 (m, 3H), 1.74-1.95 (m, 2H), 1.96-2.24 (m, 1.6H), 2.34-2.45 (m, 0.4H), 2.86-3.32 (m, 6H), 3.87-4.08 (m, 4H), 4.18-4.32 (m, 1.4H), 4.34-4.60 (m, 2H), 4.72-4.82 (m, 0.6H), 4.90-5.14 (m, 1.6H), 6.06 (s, 0.6H), 6.10 (s, 0.4H), 6.27 (s, 0.6H), 6.33-6.38 (m, 0.4H), 6.60 (s, 0.4H), 6.80-6.90 (m, 1H), 6.97-7.10 (m, 2H), 7.78 (d, J = 8.70 Hz, 0.4H), 8.96 (d, J = 7.90 Hz, 0.6H), HRMS ESI/APCI dual m/z calcd for C26H30FN7O3 [M+H]+ 508.2467, found: 508.2450

Reference： [1]Yamaguchi-Sasaki, Toru; Kawaguchi, Takanori; Okada, Atsushi; Tokura, Seiken; Tanaka-Yamamoto, Nozomi; Takeuchi, Tomoki; Ogata, Yuya; Takahashi, Ryo; Kurimoto-Tsuruta, Risa; Tamaoki, Tomokazu; Sugaya, Yutaka; Abe-Kumasaka, Tomoko; Arikawa, Kaho; Yoshida, Ippei; Sugiyama, Hiroyuki; Kanuma, Kosuke; Yoshinaga, Mitsukane [Bioorganic and Medicinal Chemistry, 2020, vol. 28, # 24]

3
[ 50-00-0 ]
tert-butyl N-(3-iodocyclobutyl)carbamate [ No CAS ]
[ 130369-05-0 ]
[ 142733-64-0 ]

Yield	Reaction Conditions	Operation in experiment
	With (4s,6s)-2,4,5,6-tetra(9H-carbazol-9-yl)isophthalonitrile; N-ethyl-N,N-diisopropylamine In water; acetonitrile at 20℃; for 16h; Irradiation; Overall yield = 83 percent;

Reference： [1]Caiger, Lewis; Constantin, Timothée; Douglas, James J.; Juliá, Fabio; Leonori, Daniele; Sheikh, Nadeem S.; Sinton, Conar [Chemical Science, 2021, vol. 12, # 31, p. 10448 - 10454]

4
tert-butyl N-(3-iodocyclobutyl)carbamate [ No CAS ]
[ 29110-74-5 ]
C₁₆H₂₀ClN₃O₂ [ No CAS ]

Yield	Reaction Conditions	Operation in experiment
93%	With tributyl-amine; trimethylsilyl(cumyl) peroxide; N,N,N′,N′-tetramethyl-N″-tert-butylguanidine; copper(l) chloride; In acetonitrile; tert-butyl alcohol; at 20℃; for 1h;Sealed tube; Inert atmosphere;	General procedure: An oven-dry tube equipped with a stirring bar was charged with the alkyl iodide (0.20 mmol, 1.0 equiv.), the N-nucleophile (0.30 mmol, 1.5 equiv.) and [Cu(MeCN)4]PF6 (7.5 mg, 0.020 mmol, 10 mol%). The tube was capped with a Supelco aluminium crimp seal with septum (PTFE/butyl) and evacuated and refilled with N2 (three times). Dry and degassed CH3CN (1.0 ml), t-BuOH (1.0 ml), (n-Bu)3N (238 μl, 1.0 mmol, 5.0 equiv.), BTMG (80 μl, 0.40 mmol, 2.0 equiv.) were sequentially added. The resulting solution was treated with cumOOTMS (224 mg, 238 μl, 1.00 mmol, 5.0 equiv.) dropwise under vigorous stirring. After 1 h the tube was opened and the mixture diluted with brine (2 ml) and EtOAc (2 ml). The organic layer was separated and the aqueous layer was extracted with EtOAc (5 ml × 2). The combined organic layers were dried (MgSO4), filtered and evaporated. The crude material was purified by flash column chromatography on silica gel.

Reference： [1]Nature Catalysis,2021,vol. 4,p. 623 - 630

5
[ 130233-77-1 ]
[ 1824239-57-7 ]

Yield	Reaction Conditions	Operation in experiment
	Multi-step reaction with 4 steps 1: Caswell No_. 744A / water monomer; acetone / 0 °C 2: toluene / 90 °C / Inert atmosphere 3: sodium tetrahydridoborate; methanol / tetrahydrofuran / 1 h / 0 - 20 °C 4: iodine; triphenylphosphine; 1H-imidazole / dichloromethane / 12 h / 20 °C

Reference： [1]Current Patent Assignee: SHEARN NANCE GALEN PAUL; SINZ CHRISTOPHER J; MERCK & CO INC; LOMBARDO MATTHEW J; HICKS JACQUELINE D; CHENG ALAN C - WO2022/10828, 2022, A1

6
[ 23761-23-1 ]
[ 1824239-57-7 ]

Yield	Reaction Conditions	Operation in experiment
	Multi-step reaction with 5 steps 1: thionyl chloride / dichloromethane / 0 °C / Reflux 2: Caswell No_. 744A / water monomer; acetone / 0 °C 3: toluene / 90 °C / Inert atmosphere 4: sodium tetrahydridoborate; methanol / tetrahydrofuran / 1 h / 0 - 20 °C 5: iodine; triphenylphosphine; 1H-imidazole / dichloromethane / 12 h / 20 °C

Reference： [1]Current Patent Assignee: SHEARN NANCE GALEN PAUL; SINZ CHRISTOPHER J; MERCK & CO INC; LOMBARDO MATTHEW J; HICKS JACQUELINE D; CHENG ALAN C - WO2022/10828, 2022, A1

7
[ 1448310-28-8 ]
[ 1824239-57-7 ]

Yield	Reaction Conditions	Operation in experiment
	Multi-step reaction with 3 steps 1: toluene / 90 °C / Inert atmosphere 2: sodium tetrahydridoborate; methanol / tetrahydrofuran / 1 h / 0 - 20 °C 3: iodine; triphenylphosphine; 1H-imidazole / dichloromethane / 12 h / 20 °C

Reference： [1]Current Patent Assignee: SHEARN NANCE GALEN PAUL; SINZ CHRISTOPHER J; MERCK & CO INC; LOMBARDO MATTHEW J; HICKS JACQUELINE D; CHENG ALAN C - WO2022/10828, 2022, A1

8
[ 154748-49-9 ]
[ 1824239-57-7 ]

Yield	Reaction Conditions	Operation in experiment
	Multi-step reaction with 2 steps 1: sodium tetrahydridoborate; methanol / tetrahydrofuran / 1 h / 0 - 20 °C 2: iodine; triphenylphosphine; 1H-imidazole / dichloromethane / 12 h / 20 °C

Reference： [1]Current Patent Assignee: SHEARN NANCE GALEN PAUL; SINZ CHRISTOPHER J; MERCK & CO INC; LOMBARDO MATTHEW J; HICKS JACQUELINE D; CHENG ALAN C - WO2022/10828, 2022, A1

9
[ 154748-63-7 ]
[ 1824239-57-7 ]

Yield	Reaction Conditions	Operation in experiment
	With 1H-imidazole; iodine; triphenylphosphine In dichloromethane at 20℃; for 12h;	Step 5. tert-butyl (3-iodocyclobutyl)carbamate: To a solution of tert-butyl N-(3- hydroxycyclobutyl)carbamate (88.9 g, 472.8 mmol, 1.0 eq) in DCM (900 mL) was added I2 (144 g, 567.4 mmol, 1.2 eq), PPh3(148.6 g, 567.4 mmol, 1.2 eq), and imidazole (38.6 g, 567.4 mmol, 1.2 eq). The reaction mixture was stirred at rt 12h. The mixture was diluted with 2L H2O, then filtered, and the liquid was extracted with DCM(2x1L). The organic layers were combined and washed with brine (2 ×1 L). The organic layer was dried by Na2SO4 and concentrated under vacuum. The residue was purified by flash silica gel chromatography (3% ethyl acetate/ petroleum ether) to afford the title compound

Reference： [1]Current Patent Assignee: SHEARN NANCE GALEN PAUL; SINZ CHRISTOPHER J; MERCK & CO INC; LOMBARDO MATTHEW J; HICKS JACQUELINE D; CHENG ALAN C - WO2022/10828, 2022, A1 Location in patent: Page/Page column 36

10
[ 57381-49-4 ]
[ 1824239-57-7 ]
[ 2758093-20-6 ]
[ 2758093-24-0 ]

Yield	Reaction Conditions	Operation in experiment
	With [2,2]bipyridinyl; nickel(II) chloride ethylene glycol dimethyl ether complex; N,N,N-tributyl-1-butanaminium iodide; zinc powder In N,N-dimethyl acetamide at 27℃; for 12h;	Step 1. tert-butyl ((cis)-3-(4-chloropyridin-2-yl)cyclobutyl)carbamate: To a solution of 2,2'-bipyridine (0.105 g, 0.673 mmol), nickel(II) chloride ethylene glycol dimethyl ether complex (0.148 g, 0.673 mmol), TBAI (1.243 g, 3.37 mmol) and zinc (0.330 g, 5.05 mmol) in DMA (5 mL) was added tert-butyl (3-iodocyclobutyl)carbamate (1 g, 3.37 mmol) and 2-bromo- 4-chloropyridine (0.648 g, 3.37 mmol) at 27°C. The mixture was stirred at 27°C for 12 h. Water was added and the reaction was extracted with EtOAc. The organic layers were concentrated and purified by flash silica gel chromatography (0-40% Pet. ether/EtOAc gradient) to give the title compound as a mixture of cis and trans isomers. The isomers were separated by SFC (OD- H; Mobile 15% EtOH (0.1% NH3H2O)) to provide the faster eluting isomer tert-butyl ((cis)-3-(4- chloropyridin-2-yl)cyclobutyl)carbamate and the slower eluting isomer tert-butyl ((trans)-3-(4- chloropyridin-2-yl)cyclobutyl)carbamate

11
[ 57381-49-4 ]
[ 1824239-57-7 ]
[ 2758092-69-0 ]
[ CAS Unavailable ]

Yield	Reaction Conditions	Operation in experiment
	With [2,2]bipyridinyl; nickel(II) chloride ethylene glycol dimethyl ether complex; zinc powder In N,N-dimethyl acetamide at 25℃; for 3h; Inert atmosphere;	Step 6. tert-butyl (3-(5-chloro-2-cyanophenyl)cyclobutyl)carbamate: To a solution of NiCl2(DME) (16.25 g, 73.97 mmol, 0.2 eq) in DMA (1000 mL) was added, DPy (11.55 g, 73.97 mmol, 0.2 eq) and the mixture was degassed with N2 (x3) and stirred at room temperature for 30 min. tert-butyl N-(3-iodocyclobutyl)carbamate (109.9 g, 369.86 mmol, 1.0 eq), 2-bromo-4- chlorobenzonitrile (96.07 g, 443.84 mmol, 1.2 eq), and zinc powder (36.29 g, 554.8 mmol, 1.5 eq) in DMA (4000 mL )was added. The mixture was degassed with N2 (x3). The reaction mixture was stirred at r.t for 3 h and 5 L of water was added. The resulting solution was extracted with ethyl acetate(3 x 2 L) and the organic layers combined. The resulting mixture was washed with brine. The organic layers were dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was purified by flash silica gel chromatography (2% to 3% ethyl acetate/ petroleum ether) to afford mixture of isomers. The title compounds were resolved by Prep-SFC with the following conditions: EnantioPak-A1-5(02); IPA 40%). This resulted in the faster eluting isomer tert-butyl (cis-(5-chloro-2- cyanophenyl)cyclobutyl)carbamate obtained as a solid: MS: 305. 1H NMR (300 MHz, CD3OD): δ 7.66 (d, J = 8.3 Hz, 1H), 7.57 (d, J = 1.9 Hz, 1H), 7.41 (dd, J = 8.3, 2.0 Hz, 1H), 4.10 (p, J = 8.3 Hz, 1H), 3.48 (tt, J = 10.1, 7.6 Hz, 1H), 2.92 - 2.74 (m, 2H), 2.18 - 2.01 (m, 2H), 1.46 (s, 9H). [M-1]-. The slower eluting isomer tert-butyl (trans-(5-chloro-2- cyanophenyl)cyclobutyl)carbamate obtained as a solid: MS: 305 [M-1] 1H NMR (300 MHz, CD3OD): δ 7.69 (d, J = 8.2 Hz, 2H), 7.42 (dd, J = 8.3, 2.0 Hz, 1H), 4.17 (dt, J = 14.2, 6.4 Hz, 1H), 3.91 (p, J = 7.6, 7.2 Hz, 1H), 2.54 (t, J = 7.3 Hz, 4H), 1.47 (s, 9H).

12
[ 1824239-57-7 ]
[ 3128-77-6 ]
[ CAS Unavailable ]

Yield	Reaction Conditions	Operation in experiment
	With tributyl-amine; (4s,6s)-2,4,5,6-tetra(9H-carbazol-9-yl)isophthalonitrile In ethyl acetate at 30℃; for 12h; Sealed tube; Inert atmosphere; Irradiation;

Reference： [1]Kumar, Amit; Rizwana Rahmathulla, A.; Tripathy, Alisha Rani; Yatham, Veera Reddy [Organic and Biomolecular Chemistry, 2022, vol. 20, # 15, p. 3136 - 3144]

13
[ 33675-41-1 ]
[ 1824239-57-7 ]
[ CAS Unavailable ]

Yield	Reaction Conditions	Operation in experiment
69%	With tributyl-amine; (4s,6s)-2,4,5,6-tetra(9H-carbazol-9-yl)isophthalonitrile In ethyl acetate at 30℃; for 24h; Inert atmosphere; Sealed tube; Irradiation;

Reference： [1]Tripathy, Alisha Rani; Kumar, Amit; Rahmathulla A, Rizwana; Jha, Avishek Kumar; Yatham, Veera Reddy [Organic Letters, 2022, vol. 24, # 28, p. 5186 - 5191]

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Technical Information

• 1,4-Addition of an Amine to a Conjugated Enone • 1,4-Addition of an Amine to a Conjugated Enone • Acid-Catalyzed α -Halogenation of Ketones • Acyl Group Substitution • Alcohols Convert Acyl Chlorides into Esters • Alcohols from Haloalkanes by Acetate Substitution-Hydrolysis • Alcohols React with PX3 • Alcoholysis of Anhydrides • Alkyl Halide Occurrence • Amide Hydrolysis • Amide Hydrolysis • Amides Can Be Converted into Aldehydes • Amine Synthesis from Nitriles • Amine Synthesis from Nitriles • Amines Convert Acyl Chlorides into Amides • Amines Convert Esters into Amides • Azide Reduction by LiAlH4 • Azide Reduction by LiAlH4 • Basicity of Amines • Bouveault-Blanc Reduction • Buchwald-Hartwig C-N Bond and C-O Bond Formation Reactions • Catalytic Hydrogenation • Chan-Lam Coupling Reaction • Chichibabin Reaction • Claisen Condensations Produce β-Dicarbonyl Compounds • Claisen Condensations Produce β-Dicarbonyl Compounds • Complex Metal Hydride Reductions • Convert Esters into Aldehydes Using a Milder Reducing Agent • Convert Haloalkanes into Alcohols by SN2 • Decarboxylation of 3-Ketoacids Yields Ketones • Deprotection of Cbz-Amino Acids • Diazotization Reaction • DIBAL Attack Nitriles to Give Ketones • Enamine Formation • Ester Cleavage • Ester Hydrolysis • Formation of an Amide from an Amine and a Carboxylic Acid • Formation of an Amide from an Amine and a Carboxylic Acid • Friedel-Crafts Alkylation of Benzene with Haloalkanes • General Reactivity • Grignard Reagents Transform Esters into Alcohols • Halogenation • Hantzsch Pyridine Synthesis • Heat of Combustion • Hemiaminal Formation from Amines and Aldehydes or Ketones • Hemiaminal Formation from Amines and Aldehydes or Ketones • Hiyama Cross-Coupling Reaction • Hofmann Elimination • Hofmann Rearrangement • Hydride Reductions • Hydrolysis of Imines to Aldehydes and Ketones • Imine Formation from Amines and Aldehydes or Ketones • Ketones Undergo Mixed Claisen Reactions to Form β-Dicarbonyl Compounds • Kinetics of Alkyl Halides • Lawesson's Reagent • Leuckart-Wallach Reaction • Mannich Reaction • Methylation of Ammonia • Methylation of Ammonia • Nitrosation of Amines • Peptide Bond Formation with DCC • Petasis Reaction • Preparation of Amines • Preparation of LDA • Reactions of Alkyl Halides with Reducing Metals • Reactions of Amines • Reactions of Dihalides • Reactions with Organometallic Reagents • Reduction of an Amide to an Amine • Reduction of an Amide to an Amine • Reduction of an Ester to an Alcohol • Reduction of an Ester to an Aldehyde • Reductive Amination • Reductive Amination • Ring Opening of Azacyclopropanes • Ring Opening of Azacyclopropanes • Ring Opening of Oxacyclobutanes • Specialized Acylation Reagents-Carbodiimides and Related Reagents • Specialized Acylation Reagents-Ketenes • Specialized Acylation Reagents-Vilsmeier Reagent • Strecker Synthesis • Substitution and Elimination Reactions of Alkyl Halides • Suzuki Coupling • Synthesis of 2-Amino Nitriles • The Cycloaddition of Dienes to Alkenes Gives Cyclohexenes • Transesterification • Ugi Reaction

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Ghs Precautionary Statements

Precautionary Statements-General
Code	Phrase
P101	If medical advice is needed,have product container or label at hand.
P102	Keep out of reach of children.
P103	Read label before use
Prevention
Code	Phrase
P201	Obtain special instructions before use.
P202	Do not handle until all safety precautions have been read and understood.
P210	Keep away from heat/sparks/open flames/hot surfaces. - No smoking.
P211	Do not spray on an open flame or other ignition source.
P220	Keep/Store away from clothing/combustible materials.
P221	Take any precaution to avoid mixing with combustibles
P222	Do not allow contact with air.
P223	Keep away from any possible contact with water, because of violent reaction and possible flash fire.
P230	Keep wetted
P231	Handle under inert gas.
P232	Protect from moisture.
P233	Keep container tightly closed.
P234	Keep only in original container.
P235	Keep cool
P240	Ground/bond container and receiving equipment.
P241	Use explosion-proof electrical/ventilating/lighting/equipment.
P242	Use only non-sparking tools.
P243	Take precautionary measures against static discharge.
P244	Keep reduction valves free from grease and oil.
P250	Do not subject to grinding/shock/friction.
P251	Pressurized container: Do not pierce or burn, even after use.
P260	Do not breathe dust/fume/gas/mist/vapours/spray.
P261	Avoid breathing dust/fume/gas/mist/vapours/spray.
P262	Do not get in eyes, on skin, or on clothing.
P263	Avoid contact during pregnancy/while nursing.
P264	Wash hands thoroughly after handling.
P265	Wash skin thouroughly after handling.
P270	Do not eat, drink or smoke when using this product.
P271	Use only outdoors or in a well-ventilated area.
P272	Contaminated work clothing should not be allowed out of the workplace.
P273	Avoid release to the environment.
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

Purity	Size	Price	VIP Price	USA Stock *0-1 Day	Global Stock *5-7 Days	Quantity
{[ item.p_purity ]}	{[ item.pr_size ]}	Inquiry	{[ getRatePrice(item.pr_usd, 1,1,item.pr_is_large_size_no_price) ]} {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price) ]}	{[ getRatePrice(item.pr_usd, 1,1,item.pr_is_large_size_no_price) ]}	Inquiry {[ getRatePrice(item.pr_usd,item.pr_rate,item.mem_rate,item.pr_is_large_size_no_price) ]} {[ getRatePrice(item.pr_usd,1,item.mem_rate,item.pr_is_large_size_no_price) ]}	{[ item.pr_usastock ]}		{[ item.pr_chinastock ]}	{[ item.pr_remark ]}

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

[ CAS No. 1824239-57-7 ] {[proInfo.proName]}

Quality Control of [ 1824239-57-7 ]

Related Doc. of [ 1824239-57-7 ]

Product Details of [ 1824239-57-7 ]

Calculated chemistry of [ 1824239-57-7 ] Expand+

Physicochemical Properties

Pharmacokinetics

Lipophilicity

Druglikeness

Water Solubility

Medicinal Chemistry

Safety of [ 1824239-57-7 ]

Application In Synthesis of [ 1824239-57-7 ]

[ 1824239-57-7 ] Synthesis Path-Downstream 1~13

Technical Information

Related Functional Groups of [ 1824239-57-7 ]

Aliphatic Cyclic Hydrocarbons

Amides

Amines

Precautionary Statements-General

Prevention

Response

Storage

Disposal

Physical hazards

Health hazards

Environmental hazards

Inquiry

Related Functional Groups of
[ 1824239-57-7 ]