tert-butyl (2-bromothiazol-4-yl)carbamate

tert-butyl (2-bromothiazol-4-yl)carbamate

ethyl 2-bromo-4-(trifluoromethyl)thiazole-5-carboxylate

ethyl 2-bromo-4-(trifluoromethyl)thiazole-5-carboxylate

2-bromothiazol-4-amine hydrobromide

$200.00
CAS No.: 41731-35-5
Catalog No.: 196084
Purity: 95%
MF: C3H4Br2N2S
MW: 259.954
Storage: 2-8 degree Celsius
SMILES: Br.BrC=1SC=C(N1)N
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196084
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2-bromothiazol-4-amine hydrobromide; CAS No.: 41731-35-5; 2-bromothiazol-4-amine hydrobromide. PROPERTIES: 2-bromothiazol-4-amine hydrobromide is a crystalline salt with a molecular weight of approximately 242.0 g/mol. It has a melting point around 180-185 C (decomposition). The compound is highly water-soluble due to the hydrobromide salt form but has limited solubility in organic solvents. The amine group is fully protonated in the hydrobromide form. For proper storage, keep in a tightly sealed container at room temperature away from heat and moisture. Safety: This compound may cause skin corrosion and serious eye damage. In case of accidental ingestion, rinse mouth immediately and seek medical advice. Use only in well-ventilated areas and avoid contact with foodstuffs. APPLICATIONS: In pharmaceutical research, 2-bromothiazol-4-amine hydrobromide serves as a building block for creating antimicrobial agents. The bromine substituent enhances penetration through microbial cell walls. In organic synthesis, it is used as a starting material for creating heterocyclic compounds via nucleophilic substitution reactions. The amine group participates in condensation reactions to form larger ring systems. In materials science, derivatives of this compound are explored for creating conductive polymers. The thiazole ring and the amine group provide structural features that enhance electrical conductivity. These applications are supported by research in medicinal chemistry journals and polymer science publications.

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