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.

Properties

• CAS Number: 1934494-58-2
• Complexity: 167
• IUPAC Name: N-(4-bromo-5-methyl-thiazol-2-yl)acetamide
• InChI: InChI=1S/C6H7BrN2OS/c1-3-5(7)9-6(11-3)8-4(2)10/h1-2H3,(H,8,9,10)
• InChI Key: NYHMMODGUQWDNP-UHFFFAOYSA-N
• Exact Mass: 233.94625
• Molecular Formula: C6H7BrN2OS
• Molecular Weight: 235.10
• SMILES: CC1=C(N=C(S1)NC(=O)C)Br
• Topological: 70.2
• Monoisotopic Mass: 233.94625
• 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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