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Atomfair N-(4-Bromo-5-methylthiazol-2-yl)acetamide C6H7BrN2OS
Description N-(4-Bromo-5-methylthiazol-2-yl)acetamide (CAS No. 1934494-58-2) is a high-purity brominated thiazole derivative with the molecular formula C6H7BrN2OS . This specialized compound is designed for advanced research applications, particularly in medicinal chemistry and pharmaceutical development. The presence of both bromine and acetamide functional groups on the thiazole ring makes it a valuable intermediate for synthesizing novel heterocyclic compounds. Our product is rigorously tested to ensure ??95% purity (HPLC) and is supplied as a crystalline solid with full characterization data including1H NMR,13C NMR, and mass spectrometry. Ideal for: ? Structure-activity relationship studies ? Fragment-based drug discovery ? Cross-coupling reactions ? Thiazole scaffold modifications.…
Description
Description
N-(4-Bromo-5-methylthiazol-2-yl)acetamide (CAS No. 1934494-58-2) is a high-purity brominated thiazole derivative with the molecular formula C6H7BrN2OS. This specialized compound is designed for advanced research applications, particularly in medicinal chemistry and pharmaceutical development. The presence of both bromine and acetamide functional groups on the thiazole ring makes it a valuable intermediate for synthesizing novel heterocyclic compounds. Our product is rigorously tested to ensure ??95% purity (HPLC) and is supplied as a crystalline solid with full characterization data including 1H NMR, 13C NMR, and mass spectrometry. Ideal for: ? Structure-activity relationship studies ? Fragment-based drug discovery ? Cross-coupling reactions ? Thiazole scaffold modifications. Store in a cool, dry place at 2-8??C under inert atmosphere for maximum stability.
- CAS No: 1934494-58-2
- Molecular Formula: C6H7BrN2OS
- Molecular Weight: 235.10
- Exact Mass: 233.94625
- Monoisotopic Mass: 233.94625
- IUPAC Name: N-(4-bromo-5-methyl-1,3-thiazol-2-yl)acetamide
- SMILES: CC1=C(N=C(S1)NC(=O)C)Br
- Synonyms: N-(4-Bromo-5-methylthiazol-2-yl)acetamide, 1934494-58-2, N-(4-Bromo-5-methyl-1,3-thiazol-2-yl)acetamide
Application
N-(4-Bromo-5-methylthiazol-2-yl)acetamide serves as a key building block in medicinal chemistry for developing thiazole-containing drug candidates. The bromine substituent enables versatile cross-coupling reactions for structural diversification. Researchers utilize this compound to study kinase inhibition and antimicrobial activity in thiazole derivatives. Its electron-deficient thiazole core facilitates nucleophilic substitution reactions for creating combinatorial libraries.
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