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CN
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安全信息

217344

Sigma-Aldrich

三氯乙酰胺

99%

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About This Item

线性分子式:
Cl3CCONH2
CAS号:
594-65-0
分子量:
162.40
Beilstein:
1754028
EC 号:
209-849-3
MDL编号:
MFCD00008009
UNSPSC代码:
12352100
PubChem化学物质编号:
24853011

方案

99%

表单

solid

沸点

238-240 °C (lit.)

mp

139-141 °C (lit.)

SMILES字符串

NC(=O)C(Cl)(Cl)Cl

InChI

1S/C2H2Cl3NO/c3-2(4,5)1(6)7/h(H2,6,7)

InChI key

UPQQXPKAYZYUKO-UHFFFAOYSA-N

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一般描述

三氯乙酰胺是三氯乙腈的主要降解产物 。

应用

将三氯乙酰胺用于基于芯片的转录组学和基于一维质子核磁共振的代谢组学，探讨三氯乙酰胺含氮消毒副产物对小鼠的健康影响 。

象形图

Exclamation mark
GHS07

警示用语：

Warning

危险声明

H319

预防措施声明

P305 + P351 + P338

危险分类

Eye Irrit. 2

储存分类代码

13 - Non Combustible Solids

WGK

WGK 3

闪点(°F)

Not applicable

闪点(°C)

Not applicable

个人防护装备

dust mask type N95 (US), Eyeshields, Gloves

法规信息

新产品

历史批次信息供参考:

分析证书(COA)

Lot/Batch Number
MKAA3981V
1410277V
1410277
11518MH
01007BW

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Chan Lan Chun et al.
Environmental science & technology, 41(5), 1615-1621 (2007-04-03)
Disinfection byproducts (DBPs) in drinking water flowing through corroded iron or steel pipes may encounter carbonate green rust (GR(CO32-)), a mixed Fe(II)/Fe(lll) hydroxide mineral and potent reductant. This research was performed to investigate the kinetics and pathways of the degradation
Nathaniel H Park et al.
Organic letters, 11(11), 2433-2436 (2009-05-29)
A new method for the stereoselective synthesis of alpha-glycosyl ureas, via nickel-catalyzed [1,3]-rearrangement of glycosyl trichloroacetimidates, has been developed. The alpha-stereoselectivity at the anomeric carbon of the resulting trichloroacetamides depends on the nature of the cationic nickel catalyst. This method
Shih-Sheng Chang et al.
Carbohydrate research, 344(4), 432-438 (2009-01-10)
A practical and efficient alpha-selective aromatic glycosylation with simple per-O-acetyl glycopyranosyl trichloroacetimidates is reported. The method is particularly effective for L-fucosyl and 2-azido-2-deoxy-D-galatosaminyl imidates, with which exclusive alpha-selectivity was achieved. The synthetic utility of this method was demonstrated in the
Zheng Liu et al.
Organic letters, 12(13), 2974-2977 (2010-06-04)
Stereocontrolled syntheses of alpha-C-GalCer (2) and its alpha-C-acetylenic analogue 6 were accomplished in high efficiency by a convergent construction strategy from 1-hexadecene and d-galactose. The key transformations include Sonogashira coupling, Sharpless asymmetric epoxidation, and Et(2)AlCl-catalyzed cyclization of an epoxytrichloroacetimidate to
Jeffrey S Arnold et al.
Journal of the American Chemical Society, 134(20), 8380-8383 (2012-05-09)
The rhodium-catalyzed regio- and enantioselective amination of racemic tertiary allylic trichloroacetimidates with a variety of aniline nucleophiles is a direct and efficient route to chiral α,α-disubstituted allylic N-arylamines. We describe the first dynamic kinetic asymmetric transformations of racemic tertiary allylic
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