217344
三氯乙酰胺
99%
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关于此项目
线性分子式:
Cl3CCONH2
化学文摘社编号:
分子量:
162.40
EC Number:
209-849-3
UNSPSC Code:
12352100
PubChem Substance ID:
Beilstein/REAXYS Number:
1754028
MDL number:
InChI key
UPQQXPKAYZYUKO-UHFFFAOYSA-N
InChI
1S/C2H2Cl3NO/c3-2(4,5)1(6)7/h(H2,6,7)
SMILES string
NC(=O)C(Cl)(Cl)Cl
assay
99%
form
solid
bp
238-240 °C (lit.)
mp
139-141 °C (lit.)
General description
三氯乙酰胺是三氯乙腈的主要降解产物 。
Application
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 。
signalword
Warning
hcodes
pcodes
Hazard Classifications
Eye Irrit. 2
存储类别
13 - Non Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
法规信息
新产品
此项目有
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
A E Christina et al.
Carbohydrate research, 356, 282-287 (2012-03-16)
Reported is the gram-scale synthesis of tert-butyldiphenylsilyl 4-(N-benzyloxycarbonyl)-amino-2-azido-2,4,6-trideoxy-β-D-galactopyranoside, which represents an orthogonally protected 2,4-diamino-D-fucose building block, a common constituent of various zwitterionic polysaccharides. The building block has been synthesized from D-glucosamine in 19% overall yield over 14 steps, requiring 5
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
Ophélie Milhomme et al.
Carbohydrate research, 356, 115-131 (2012-02-24)
The synthesis of the anthrax tetrasaccharide, amenable for conjugation, has been envisaged by both [2+2] and [1+3] approaches from D-fucose and L-rhamnose. The successful route reported herein relies on a [1+3] strategy in which the 1,2-trans-glycosidic linkages have been secured
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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