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Atomfair 5-Bromoquinoline-8-carbonitrile C10H5BrN2

Description 5-Bromoquinoline-8-carbonitrile (CAS No. 507476-70-2) is a high-purity heterocyclic organic compound with the molecular formula C10H5BrN2. This specialized quinoline derivative features a bromo substituent at the 5-position and a cyano group at the 8-position, making it a valuable intermediate for pharmaceutical and materials science research. The compound is supplied as a crystalline solid with ??95% purity (HPLC) and is rigorously tested for consistency in quality. Ideal for cross-coupling reactions, functional group transformations, and as a building block for complex molecular architectures. Packaged under inert gas to ensure stability and shipped with comprehensive analytical data (NMR, MS, HPLC).

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Description

Description

5-Bromoquinoline-8-carbonitrile (CAS No. 507476-70-2) is a high-purity heterocyclic organic compound with the molecular formula C10H5BrN2. This specialized quinoline derivative features a bromo substituent at the 5-position and a cyano group at the 8-position, making it a valuable intermediate for pharmaceutical and materials science research. The compound is supplied as a crystalline solid with ??95% purity (HPLC) and is rigorously tested for consistency in quality. Ideal for cross-coupling reactions, functional group transformations, and as a building block for complex molecular architectures. Packaged under inert gas to ensure stability and shipped with comprehensive analytical data (NMR, MS, HPLC).

  • CAS No: 507476-70-2
  • Molecular Formula: C10H5BrN2
  • Molecular Weight: 233.06
  • Exact Mass: 231.96361
  • Monoisotopic Mass: 231.96361
  • IUPAC Name: 5-bromoquinoline-8-carbonitrile
  • SMILES: C1=CC2=C(C=CC(=C2N=C1)C#N)Br
  • Synonyms: 5-bromoquinoline-8-carbonitrile, 507476-70-2, DTXSID10460934, DTXCID00411753, 826-631-9

Application

5-Bromoquinoline-8-carbonitrile serves as a versatile precursor in medicinal chemistry for the synthesis of quinoline-based drug candidates, particularly in antiviral and anticancer research. Its bromo and cyano functional groups enable efficient participation in palladium-catalyzed cross-coupling reactions (e.g., Suzuki, Heck). Researchers also utilize it to develop luminescent materials and ligands for catalytic systems. The electron-withdrawing cyano group enhances its utility in nucleophilic aromatic substitution reactions.

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