Atomfair 2-Amino-6-fluorobenzonitrile C7H5FN2

Description 2-Amino-6-fluorobenzonitrile (CAS No. 115661-37-5) is a high-purity fluorinated aromatic nitrile compound with the molecular formula C7H5FN2. This fine chemical is characterized by its amino and cyano functional groups ortho to a fluorine substituent, making it a versatile intermediate in pharmaceutical and agrochemical synthesis. Provided as an off-white to light yellow crystalline powder, it is rigorously tested for identity (FTIR, NMR), purity (HPLC ??98%), and trace solvents (GC) to meet research-grade standards. Optimized for stability, it is packaged under inert gas in amber glass vials with PTFE-lined caps to prevent moisture absorption and degradation. Suitable for use in Suzuki couplings,…

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Description

Description

2-Amino-6-fluorobenzonitrile (CAS No. 115661-37-5) is a high-purity fluorinated aromatic nitrile compound with the molecular formula C7H5FN2. This fine chemical is characterized by its amino and cyano functional groups ortho to a fluorine substituent, making it a versatile intermediate in pharmaceutical and agrochemical synthesis. Provided as an off-white to light yellow crystalline powder, it is rigorously tested for identity (FTIR, NMR), purity (HPLC ??98%), and trace solvents (GC) to meet research-grade standards. Optimized for stability, it is packaged under inert gas in amber glass vials with PTFE-lined caps to prevent moisture absorption and degradation. Suitable for use in Suzuki couplings, palladium-catalyzed aminations, and other C-N bond-forming reactions.

  • CAS No: 115661-37-5
  • Molecular Formula: C7H5FN2
  • Molecular Weight: 136.13
  • Exact Mass: 136.04367633
  • Monoisotopic Mass: 136.04367633
  • IUPAC Name: 2-amino-6-fluorobenzonitrile
  • SMILES: C1=CC(=C(C(=C1)F)C#N)N
  • Synonyms: 2-Amino-6-fluorobenzonitrile, 77326-36-4, EC 616-451-7, DTXSID10335032, DTXCID60286121

Application

2-Amino-6-fluorobenzonitrile serves as a key building block in medicinal chemistry for developing kinase inhibitors and CNS-active compounds. Its electron-deficient aromatic ring facilitates nucleophilic aromatic substitutions in API synthesis. Researchers utilize it to construct fused heterocycles like quinazolines and benzimidazoles. The fluorine moiety enables radiofluorination studies in PET tracer development.

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