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Atomfair 7,8-Difluoro-2-methylquinolin-3-ol C10H7F2NO

Description 7,8-Difluoro-2-methylquinolin-3-ol (CAS No. 1314012-50-4) is a high-purity fluorinated quinoline derivative with the molecular formula C10H7F2NO . This compound features a quinoline backbone substituted with two fluorine atoms at the 7- and 8-positions, a methyl group at the 2-position, and a hydroxyl group at the 3-position, offering unique electronic and steric properties. Ideal for pharmaceutical research, medicinal chemistry, and material science applications, this building block is characterized by its high reactivity and potential as a ligand or intermediate in heterocyclic synthesis. Supplied as a fine powder with ??95% purity (HPLC), it is rigorously tested for consistency and stability. Store under…

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Description

Description

7,8-Difluoro-2-methylquinolin-3-ol (CAS No. 1314012-50-4) is a high-purity fluorinated quinoline derivative with the molecular formula C10H7F2NO. This compound features a quinoline backbone substituted with two fluorine atoms at the 7- and 8-positions, a methyl group at the 2-position, and a hydroxyl group at the 3-position, offering unique electronic and steric properties. Ideal for pharmaceutical research, medicinal chemistry, and material science applications, this building block is characterized by its high reactivity and potential as a ligand or intermediate in heterocyclic synthesis. Supplied as a fine powder with ??95% purity (HPLC), it is rigorously tested for consistency and stability. Store under inert conditions at 2-8??C to maintain integrity.

  • CAS No: 1314012-50-4
  • Molecular Formula: C10H7F2NO
  • Molecular Weight: 195.16
  • Exact Mass: 195.04957017
  • Monoisotopic Mass: 195.04957017
  • IUPAC Name: 7,8-difluoro-2-methylquinolin-3-ol
  • SMILES: CC1=C(C=C2C=CC(=C(C2=N1)F)F)O
  • Synonyms: 7,8-difluoro-2-methylquinolin-3-ol, 1314012-50-4, 897-739-1, 7,8-difluoro-3-hydroxy-2-methylquinoline, SCHEMBL12487302

Application

7,8-Difluoro-2-methylquinolin-3-ol serves as a versatile intermediate in the synthesis of fluorinated quinoline-based pharmaceuticals, particularly in the development of kinase inhibitors and antimicrobial agents. Its electron-withdrawing fluorine substituents enhance binding affinity in drug-receptor interactions, making it valuable for structure-activity relationship (SAR) studies. Researchers also utilize this compound in the design of fluorescent probes and optoelectronic materials due to its conjugated aromatic system.

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