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Merck
CN

77460

Sigma-Aldrich

2-Chloroacetophenone

purum, ≥98.0% (GC)

别名:

ω-Chloroacetophenone, Phenacyl chloride

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关于此项目

线性分子式:
C6H5COCH2Cl
化学文摘社编号:
分子量:
154.59
Beilstein:
507950
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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等级

purum

质量水平

方案

≥98.0% (GC)

表单

crystals

沸点

244-245 °C (lit.)

mp

53-56 °C
54-56 °C (lit.)

密度

1.324 g/mL at 25 °C (lit.)

官能团

chloro
ketone
phenyl

SMILES字符串

ClCC(=O)c1ccccc1

InChI

1S/C8H7ClO/c9-6-8(10)7-4-2-1-3-5-7/h1-5H,6H2

InChI key

IMACFCSSMIZSPP-UHFFFAOYSA-N

基因信息

human ... PTPN6(5777)

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一般描述

2-Chloroacetophenone is an organic building block used in the synthesis of heterocyclic compounds. It has low solubility in water but can be soluble in alcohols, ethers and other organic solvents.

应用

2-Chloroacetophenone can be used in the synthesis of phenyl acetic acid by Photo-Favorskii rearrangement. It is also used in the preparation of 1-(2-chlorophenyl)ethanol via asymmetric hydrogenation reaction.

警示用语:

Danger

危险分类

Acute Tox. 2 Oral - Acute Tox. 3 Dermal - Acute Tox. 3 Inhalation - Eye Dam. 1 - Resp. Sens. 1 - Skin Irrit. 2 - STOT SE 3

靶器官

Respiratory system

储存分类代码

6.1A - Combustible acute toxic Cat. 1 and 2 / very toxic hazardous materials

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

Eyeshields, Faceshields, Gloves, type P2 (EN 143) respirator cartridges

法规信息

危险化学品
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历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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Preparation of microgel-supported chiral catalysts and their application in the asymmetric hydrogenation of aromatic ketones
Deng J, et al.
Reactive and Functional Polymers, 72, 378-382 (2012)
Experimental study of the adsorption of 2-Chloroacetophenone at the air-environmental water interface
Hao, et al.
Frontiers in environmental science., 10, 2254-2254 (2022)
Principles of coaxial illumination for photochemical reactions: Part 2. Model validation
Meir, et al.
Journal of advanced materials and processing, 2 (2020)
Ionic liquid mediated and promoted one-pot green synthesis of new isoxazolyl dihydro-1 H-indol-4 (5 H)-one derivatives at ambient temperature
Modugu, et al.
Cogent Chemistry , 3, 1318693-1318693 (2017)
Expanding the [1,2]-aryl migration to the synthesis of substituted indoles.
Tao Pei et al.
Angewandte Chemie (International ed. in English), 47(22), 4231-4233 (2008-04-30)

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