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Atomfair 8-Bromoquinoline-4-carbonitrile C10H5BrN2

Description 8-Bromoquinoline-4-carbonitrile (CAS No. 1190315-89-9) is a high-purity brominated quinoline derivative with the molecular formula C10H5BrN2. This compound features a quinoline core substituted with a bromine atom at the 8-position and a cyano group at the 4-position, making it a versatile intermediate for organic synthesis and pharmaceutical research. It is supplied as a crystalline solid with ??95% purity (HPLC), ensuring optimal performance in demanding applications. Suitable for use in cross-coupling reactions, heterocyclic chemistry, and as a building block for drug discovery, this product is rigorously tested for quality and consistency. Store in a cool, dry place under inert conditions to…

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Description

Description

8-Bromoquinoline-4-carbonitrile (CAS No. 1190315-89-9) is a high-purity brominated quinoline derivative with the molecular formula C10H5BrN2. This compound features a quinoline core substituted with a bromine atom at the 8-position and a cyano group at the 4-position, making it a versatile intermediate for organic synthesis and pharmaceutical research. It is supplied as a crystalline solid with ??95% purity (HPLC), ensuring optimal performance in demanding applications. Suitable for use in cross-coupling reactions, heterocyclic chemistry, and as a building block for drug discovery, this product is rigorously tested for quality and consistency. Store in a cool, dry place under inert conditions to maintain stability.

  • CAS No: 1190315-89-9
  • Molecular Formula: C10H5BrN2
  • Molecular Weight: 233.06
  • Exact Mass: 231.96361
  • Monoisotopic Mass: 231.96361
  • IUPAC Name: 8-bromoquinoline-4-carbonitrile
  • SMILES: C1=CC2=C(C=CN=C2C(=C1)Br)C#N
  • Synonyms: 8-bromoquinoline-4-carbonitrile, 1190315-89-9, 8-bromoquinoline- 4-carbonitrile, MFCD12024578, 8-Bromo-4-cyanoquinoline

Application

8-Bromoquinoline-4-carbonitrile is widely used as a key intermediate in the synthesis of bioactive quinoline derivatives, particularly in pharmaceutical and agrochemical research. It serves as a precursor for palladium-catalyzed cross-coupling reactions, such as Suzuki-Miyaura and Buchwald-Hartwig couplings, enabling the construction of complex heterocyclic scaffolds. Researchers also employ it in the development of fluorescent probes and coordination chemistry due to its electron-deficient quinoline core.

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