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Atomfair 8-Chloro-6-methyl-2-phenylquinoline C16H12ClN

Description 8-Chloro-6-methyl-2-phenylquinoline (CAS No. 2307-00-8) is a high-purity quinoline derivative with the molecular formula C16H12ClN . This compound features a chloro-substituted quinoline core with a methyl group at the 6-position and a phenyl ring at the 2-position, offering unique reactivity and structural versatility for synthetic applications. Ideal for researchers in medicinal chemistry, material science, and organic synthesis, this product is rigorously tested for quality (??95% purity by HPLC) and supplied in stable crystalline form under inert packaging. Suitable for use as a building block in heterocyclic synthesis, ligand design, or pharmaceutical intermediate development. Store in a cool, dry place away…

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Description

Description

8-Chloro-6-methyl-2-phenylquinoline (CAS No. 2307-00-8) is a high-purity quinoline derivative with the molecular formula C16H12ClN. This compound features a chloro-substituted quinoline core with a methyl group at the 6-position and a phenyl ring at the 2-position, offering unique reactivity and structural versatility for synthetic applications. Ideal for researchers in medicinal chemistry, material science, and organic synthesis, this product is rigorously tested for quality (??95% purity by HPLC) and supplied in stable crystalline form under inert packaging. Suitable for use as a building block in heterocyclic synthesis, ligand design, or pharmaceutical intermediate development. Store in a cool, dry place away from light and moisture.

  • CAS No: 2307-00-8
  • Molecular Formula: C16H12ClN
  • Molecular Weight: 253.72
  • Exact Mass: 253.0658271
  • Monoisotopic Mass: 253.0658271
  • IUPAC Name: 8-chloro-6-methyl-2-phenylquinoline
  • SMILES: CC1=CC2=C(C(=C1)Cl)N=C(C=C2)C3=CC=CC=C3
  • Synonyms: 8-chloro-6-methyl-2-phenylquinoline, 22960-24-3, NSC152193, DTXSID90302626, NSC-152193

Application

8-Chloro-6-methyl-2-phenylquinoline serves as a key intermediate in the synthesis of pharmacologically active quinoline derivatives, particularly in antimalarial and anticancer drug discovery. Its rigid aromatic structure makes it valuable for designing metal-chelating ligands in catalysis. Researchers also utilize this compound in the development of organic electronic materials due to its conjugated ??-system. The chloro and methyl substituents allow for further functionalization via cross-coupling or nucleophilic substitution reactions.

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