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Merck
CN

143456

Sigma-Aldrich

2-氨基-5-氯噻唑 盐酸盐

95%

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别名:
(5-Chlorothiazol-2-yl)amine hydrochloride
经验公式(希尔记法):
C3H3ClN2S · HCl
CAS号:
分子量:
171.05
EC 号:
MDL编号:
UNSPSC代码:
12352100
PubChem化学物质编号:
NACRES:
NA.22

质量水平

检测方案

95%

mp

164-167 °C (dec.) (lit.)

SMILES字符串

Cl[H].Nc1ncc(Cl)s1

InChI

1S/C3H3ClN2S.ClH/c4-2-1-6-3(5)7-2;/h1H,(H2,5,6);1H

InChI key

GTMGFQYVLSQTKP-UHFFFAOYSA-N

应用

2-Amino-5-chlorothiazole hydrochloride was used as starting reagent in the synthesis of 2-chloro-6-methylimidazo[2,1-b]thiazole.
  • Reactant for preparation of biologically active thiazole derivatives

象形图

CorrosionExclamation mark

警示用语:

Danger

危险分类

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3

靶器官

Respiratory system

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, Faceshields, Gloves

法规信息

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Aldo Andreani et al.
Bioorganic & medicinal chemistry, 12(21), 5525-5532 (2004-10-07)
In this work we describe the synthesis of a series of imidazo[2,1-b]thiazoles and 2,3-dihydroimidazo[2,1-b]thiazoles connected by means of a methylene bridge to CoQ(0). These compounds were tested as specific inhibitors of the NADH:ubiquinone reductase activity in mitochondrial membranes. The imidazothiazole

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