Atomfair Benzenecarbothioamide, 3-bromo- 3-Bromothiobenzamide C7H6BrNS

Description 3-Bromobenzenecarbothioamide (CAS No. 2227-62-5) is a high-purity organic compound with the molecular formula C7H6BrNS , widely utilized in pharmaceutical and agrochemical research. This thiobenzamide derivative features a bromine substituent at the meta-position, enhancing its reactivity in cross-coupling reactions and serving as a versatile intermediate in heterocyclic synthesis. With a molecular weight of 216.10 g/mol , it is supplied as a crystalline solid with >98% purity (HPLC), ensuring optimal performance in nucleophilic substitution, Suzuki-Miyaura couplings, and metal-catalyzed transformations. Ideal for medicinal chemistry, this compound is rigorously tested for impurities (??0.5% by GC) and packaged under inert conditions to guarantee stability.…

Description

Description

3-Bromobenzenecarbothioamide (CAS No. 2227-62-5) is a high-purity organic compound with the molecular formula C7H6BrNS, widely utilized in pharmaceutical and agrochemical research. This thiobenzamide derivative features a bromine substituent at the meta-position, enhancing its reactivity in cross-coupling reactions and serving as a versatile intermediate in heterocyclic synthesis. With a molecular weight of 216.10 g/mol, it is supplied as a crystalline solid with >98% purity (HPLC), ensuring optimal performance in nucleophilic substitution, Suzuki-Miyaura couplings, and metal-catalyzed transformations. Ideal for medicinal chemistry, this compound is rigorously tested for impurities (??0.5% by GC) and packaged under inert conditions to guarantee stability. Available in scalable quantities from milligrams to kilograms, it includes comprehensive analytical data (NMR, MS, FTIR) for quality verification.

  • CAS No: 2227-62-5
  • Molecular Formula: C7H6BrNS
  • Molecular Weight: 216.10
  • Exact Mass: 214.94043
  • Monoisotopic Mass: 214.94043
  • IUPAC Name: 3-bromobenzenecarbothioamide
  • SMILES: C1=CC(=CC(=C1)Br)C(=S)N
  • Synonyms: 3-Bromothiobenzamide, 2227-62-5, 3-Bromobenzenecarbothioamide, Benzenecarbothioamide, 3-bromo-, DTXSID40176814

Application

3-Bromobenzenecarbothioamide serves as a critical building block in the synthesis of bioactive molecules, particularly in the development of kinase inhibitors and antimicrobial agents. Its bromine moiety enables efficient participation in palladium-catalyzed cross-coupling reactions to construct complex aryl-thioamide scaffolds. Researchers also employ it as a precursor for thiazole and benzothiazole derivatives in drug discovery programs.

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