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Merck
CN

159158

Sigma-Aldrich

乙脒 盐酸盐

95%

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关于此项目

线性分子式:
CH3C(=NH)NH2 · HCl
CAS Number:
分子量:
94.54
Beilstein:
3591762
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22
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质量水平

方案

95%

表单

solid

mp

165-170 °C (lit.)

官能团

amidine

SMILES字符串

Cl[H].CC(N)=N

InChI

1S/C2H6N2.ClH/c1-2(3)4;/h1H3,(H3,3,4);1H

InChI key

WCQOBLXWLRDEQA-UHFFFAOYSA-N

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一般描述

乙脒盐酸盐是一种脒盐,已经研究了它向2,4,6-三甲基 -对称-三嗪的转化。

应用

乙脒盐酸盐被用于制备脱羧基嘌呤。 它还被用于合成4-(4-羟基苯基)亚甲基-2-甲基-5-氧代-1-咪唑乙酸乙酯。

储存分类代码

11 - 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


历史批次信息供参考:

分析证书(COA)

Lot/Batch Number

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H Niwa et al.
Proceedings of the National Academy of Sciences of the United States of America, 93(24), 13617-13622 (1996-11-26)
The jellyfish Aequorea victoria possesses in the margin of its umbrella a green fluorescent protein (GFP, 27 kDa) that serves as the ultimate light emitter in the bioluminescence reaction of the animal. The protein is made up of 238 amino
Synthesis of the sym-Triazine System. I. Trimerization and Cotrimerization of Amidines.
Schaefer FC, et al.
Journal of the American Chemical Society, 81(6), 1466-1470 (1959)
Michael Schnoor et al.
Biochemical and biophysical research communications, 322(3), 867-872 (2004-09-01)
Different substances such as dimethyl sulfoxide, tetramethylene sulfoxide, 2-pyrollidone, and the naturally occurring compatible solute betaine enhance PCR amplification of GC-rich DNA templates with high melting temperatures. In particular, cyclic compatible solutes outperform traditional PCR enhancers. We therefore investigated the
Justin E Jones et al.
Bioorganic chemistry, 38(2), 62-73 (2009-12-29)
Helicobacter pylori encodes a potential virulence factor, agmatine deiminase (HpAgD), which catalyzes the conversion of agmatine to N-carbamoyl putrescine (NCP) and ammonia - agmatine is decarboxylated arginine. Agmatine is an endogenous human cell signaling molecule that triggers the innate immune
Cristina Maccallini et al.
Medicinal chemistry (Shariqah (United Arab Emirates)), 8(6), 991-995 (2012-06-30)
A new series of phenyl- and heteryl acetamidines were synthesized and evaluated as inhibitors of nitric oxide synthases (NOS). While the N-substitution of the acetamidine moiety with different heterocycles appears to completely destroy the activity, linking the phenyl core preserves

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