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Atomfair 2-Amino-5-bromo-3-fluorobenzonitrile C7H4BrFN2

Description 2-Amino-5-bromo-3-fluorobenzonitrile (CAS No. 1209498-46-3) is a high-purity aromatic compound with the molecular formula C7H4BrFN2. This specialized chemical features a benzonitrile core substituted with amino, bromo, and fluoro functional groups, making it a valuable intermediate for pharmaceutical and agrochemical synthesis. With a molecular weight of 215.03 g/mol, it is supplied as a crystalline solid with ??95% purity (HPLC). Ideal for cross-coupling reactions, nucleophilic substitutions, and heterocycle formation, this compound is rigorously tested for consistency and stored under controlled conditions to ensure stability. Available in research quantities (100mg to 10g) with optional custom packaging. SDS and analytical data (NMR, MS, HPLC)…

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Description

Description

2-Amino-5-bromo-3-fluorobenzonitrile (CAS No. 1209498-46-3) is a high-purity aromatic compound with the molecular formula C7H4BrFN2. This specialized chemical features a benzonitrile core substituted with amino, bromo, and fluoro functional groups, making it a valuable intermediate for pharmaceutical and agrochemical synthesis. With a molecular weight of 215.03 g/mol, it is supplied as a crystalline solid with ??95% purity (HPLC). Ideal for cross-coupling reactions, nucleophilic substitutions, and heterocycle formation, this compound is rigorously tested for consistency and stored under controlled conditions to ensure stability. Available in research quantities (100mg to 10g) with optional custom packaging. SDS and analytical data (NMR, MS, HPLC) provided upon request.

  • CAS No: 1209498-46-3
  • Molecular Formula: C7H4BrFN2
  • Molecular Weight: 215.02
  • Exact Mass: 213.95419
  • Monoisotopic Mass: 213.95419
  • IUPAC Name: 2-amino-5-bromo-3-fluorobenzonitrile
  • SMILES: C1=C(C=C(C(=C1C#N)N)F)Br
  • Synonyms: 2-amino-5-bromo-3-fluorobenzonitrile, 1209498-46-3, DTXSID90676495, DTXCID30627244, 861-704-9

Application

2-Amino-5-bromo-3-fluorobenzonitrile serves as a key building block in medicinal chemistry for the development of kinase inhibitors and CNS-active compounds. Its reactive bromo and amino groups enable Suzuki-Miyaura couplings and Buchwald-Hartwig aminations. The electron-withdrawing nitrile and fluoro substituents enhance its utility in nucleophilic aromatic substitution reactions. Researchers employ this intermediate in the synthesis of fluorinated heterocycles for drug discovery programs targeting oncology and neurological disorders.

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