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Merck
CN

151599

Sigma-Aldrich

三氯乙酰氯

99%

别名:

2,2,2-三氯乙酰氯, 三氯乙酰氯

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线性分子式:
Cl3CCOCl
化学文摘社编号:
分子量:
181.83
Beilstein:
774120
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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蒸汽压

16 mmHg ( 20 °C)

质量水平

方案

99%

表单

liquid

折射率

n20/D 1.470 (lit.)

沸点

114-116 °C (lit.)

mp

−57 °C (lit.)

密度

1.629 g/mL at 25 °C (lit.)

官能团

acyl chloride
chloro

SMILES字符串

ClC(=O)C(Cl)(Cl)Cl

InChI

1S/C2Cl4O/c3-1(7)2(4,5)6

InChI key

PVFOMCVHYWHZJE-UHFFFAOYSA-N

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一般描述

氯化三氯乙酰,又称2,2,2-三氯乙酰氯,是一种不对称酮。在实验室中常用作氯原子源。也作为酰化剂制备双(三氯乙酰)环烯胺类化合物。

应用

三氯乙酰氯可用于制备二氢-1H-苯并吲哚,还用于合成3-烷基苯并恶唑酮

象形图

CorrosionExclamation mark

警示用语:

Danger

危险声明

危险分类

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1A

储存分类代码

8A - Combustible corrosive hazardous materials

WGK

WGK 3

闪点(°F)

213.8 °F - open cup

闪点(°C)

101 °C - open cup

个人防护装备

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

法规信息

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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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Rate constants at room temperature (293 ± 2 K) and atmospheric pressure for the reaction of methyl n-propyl ether (MnPE), CH
A M Saillenfait et al.
Archives of toxicology, 70(2), 71-82 (1995-01-01)
The embryotoxicity of trichloroethylene (TRI), tetrachloroethylene (PER), and of four of their oxidative metabolites i.e. trichloroacetic acid, dichloroacetic acid, chloral hydrate, and trichloroacetyl chloride, was studied in vitro, using the rat whole embryo culture system. Embryos from Sprague-Dawley rats were
Hülya Senöz et al.
Chemical & pharmaceutical bulletin, 51(4), 444-447 (2003-04-04)
The pyrrolidine and morpholine enamines of cyclic ketones such as cyclohexanone and cyclopentanone were successfully diacetylated at alpha- and alpha'-positions with trichloroacetyl chloride using zinc catalyst. Morpholine enamines of the cyclic ketones gave acetylated morpholine in good yields besides the
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The Journal of organic chemistry, 78(23), 11935-11947 (2013-10-31)
Benzoxazolone pharmacophore is present in clinical pharmaceuticals, drug candidates, and many compounds having a wide spectrum of biological activities. The methods available for the synthesis of benzoxazolones have limited diversity due to problems in accessibility and air-sensitivity of diversely substituted
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The first examples of dihydro-1H-benzindoles by enantioselective γ-lactamization reaction of naphthyl sulfilimines with trichloroacetyl chloride in the presence of ZnCu as catalyst (≥98:2 er and 65-80% yields) are described. Products are obtained by [3,3]-sigmatropic rearrangement of the azasulfonium enolate or

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