143456
2-氨基-5-氯噻唑 盐酸盐
95%
别名:
(5-Chlorothiazol-2-yl)amine hydrochloride
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关于此项目
经验公式（希尔记法）:
C3H3ClN2S · HCl
化学文摘社编号:
分子量:
171.05
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
259-680-4
MDL number:
产品名称
2-氨基-5-氯噻唑 盐酸盐, 95%
InChI key
GTMGFQYVLSQTKP-UHFFFAOYSA-N
InChI
1S/C3H3ClN2S.ClH/c4-2-1-6-3(5)7-2;/h1H,(H2,5,6);1H
SMILES string
Cl[H].Nc1ncc(Cl)s1
assay
95%
mp
164-167 °C (dec.) (lit.)
functional group
chloro
Quality Level
Application
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
signalword
Danger
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
target_organs
Respiratory system
存储类别
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Faceshields, Gloves
法规信息
新产品
此项目有
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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