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Atomfair Methyl 3-fluoro-5-methylisonicotinate C8H8FNO2

Description Methyl 3-fluoro-5-methylisonicotinate (CAS No. 1803821-90-0) is a high-purity fluorinated pyridine derivative with the molecular formula C8H8FNO2. This compound, also known as methyl 3-fluoro-5-methylpyridine-4-carboxylate, is a versatile building block in pharmaceutical and agrochemical research. Its unique structure, featuring a fluorine substituent and a methyl ester group on the pyridine ring, makes it valuable for synthesizing bioactive molecules, ligands, and intermediates. The product is rigorously tested for quality (??95% purity by HPLC) and is supplied in sealed, light-resistant packaging to ensure stability. Ideal for medicinal chemistry, cross-coupling reactions, and heterocyclic compound development.

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Description

Description

Methyl 3-fluoro-5-methylisonicotinate (CAS No. 1803821-90-0) is a high-purity fluorinated pyridine derivative with the molecular formula C8H8FNO2. This compound, also known as methyl 3-fluoro-5-methylpyridine-4-carboxylate, is a versatile building block in pharmaceutical and agrochemical research. Its unique structure, featuring a fluorine substituent and a methyl ester group on the pyridine ring, makes it valuable for synthesizing bioactive molecules, ligands, and intermediates. The product is rigorously tested for quality (??95% purity by HPLC) and is supplied in sealed, light-resistant packaging to ensure stability. Ideal for medicinal chemistry, cross-coupling reactions, and heterocyclic compound development.

  • CAS No: 1803821-90-0
  • Molecular Formula: C8H8FNO2
  • Molecular Weight: 169.15
  • Exact Mass: 169.05390666
  • Monoisotopic Mass: 169.05390666
  • IUPAC Name: methyl 3-fluoro-5-methylpyridine-4-carboxylate
  • SMILES: CC1=CN=CC(=C1C(=O)OC)F
  • Synonyms: 1803821-90-0, Methyl 3-fluoro-5-methylisonicotinate, 812-426-1, Methyl 3-fluoro-5-methylpyridine-4-carboxylate, 4-Pyridinecarboxylic acid, 3-fluoro-5-methyl-, methyl ester

Application

Methyl 3-fluoro-5-methylisonicotinate serves as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly kinase inhibitors and CNS-targeting drugs. Its reactive ester group enables facile derivatization, while the fluorine atom enhances metabolic stability in drug candidates. Researchers also utilize it in metal-catalyzed cross-coupling reactions to construct complex heterocycles. Applications extend to agrochemical development, where fluorinated pyridines improve pesticide efficacy.

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