111902
4-氯苯甲酰氯
99%
别名:
4-Chlorobenzoic acid chloride, p-Chlorobenzoyl chloride
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关于此项目
线性分子式:
ClC6H4COCl
化学文摘社编号:
分子量:
175.01
NACRES:
NA.22
PubChem Substance ID:
eCl@ss:
39050512
UNSPSC Code:
12352100
EC Number:
204-515-3
MDL number:
Beilstein/REAXYS Number:
471606
产品名称
4-氯苯甲酰氯, 99%
InChI key
RKIDDEGICSMIJA-UHFFFAOYSA-N
InChI
1S/C7H4Cl2O/c8-6-3-1-5(2-4-6)7(9)10/h1-4H
SMILES string
ClC(=O)c1ccc(Cl)cc1
assay
99%
refractive index
n20/D 1.578 (lit.)
bp
102-104 °C/11 mmHg (lit.)
mp
11-14 °C (lit.)
density
1.365 g/mL at 20 °C (lit.)
functional group
acyl chloride
chloro
Quality Level
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Application
4-氯苯甲酰氯在 KHCO3 缓冲液中与 CoA 反应合成 4-氯苯甲酰 CoA 。
General description
4-氯苯甲酰氯可用作药物合成中的中间化合物。
signalword
Danger
hcodes
Hazard Classifications
Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1B
存储类别
8A - Combustible corrosive hazardous materials
wgk
WGK 1
flash_point_f
221.0 °F - closed cup
flash_point_c
105 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
法规信息
危险化学品
此项目有
Competing intramolecular NH? OC hydrogen bonds and extended intermolecular network in 1-(4-chlorobenzoyl)-3-(2-methyl-4-oxopentan-2-yl) thiourea analyzed by experimental and theoretical methods
Saeed, Aamer, et al.
Chemical Physics, 431, 39-46 (2014)
S D Copley et al.
Applied and environmental microbiology, 58(4), 1385-1387 (1992-04-01)
4-Chlorobenzoate degradation in cell extracts of Acinetobacter sp. strain 4-CB1 occurs by initial synthesis of 4-chlorobenzoyl coenzyme A (4-chlorobenzoyl CoA) from 4-chlorobenzoate, CoA, and ATP. 4-Chlorobenzoyl CoA is dehalogenated to 4-hydroxybenzoyl CoA. Following the dehalogenation reaction, 4-hydroxybenzoyl CoA is hydrolyzed
Iteb Trabelsi et al.
Journal of oleo science, 66(7), 667-676 (2017-07-05)
The article deals with the use of mixed anhydrides for the synthesis of fatty esters. Both aliphatic and aromatic acids are involved, indicating different behaviors according to the chain length of the aliphatic acid. We describe a novel and efficient
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