143456
2-Amino-5-chlorothiazole hydrochloride
95%
Synonym(s):
(5-Chlorothiazol-2-yl)amine hydrochloride
Sign Into View Organizational & Contract Pricing
All Photos(2)
About This Item
Empirical Formula (Hill Notation):
C3H3ClN2S · HCl
CAS Number:
Molecular Weight:
171.05
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22
Recommended Products
Quality Level
Assay
95%
mp
164-167 °C (dec.) (lit.)
functional group
chloro
SMILES string
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
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
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Acute Tox. 4 Oral - Eye Dam. 1 - Skin Irrit. 2 - Skin Sens. 1 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
Not applicable
Flash Point(C)
Not applicable
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
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
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service