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Atomfair 2-Fluoro-5-methylbenzonitrile C8H6FN

Description 2-Fluoro-5-methylbenzonitrile (CAS No. 64113-84-4) is a high-purity fluorinated aromatic nitrile compound with the molecular formula C8H6FN. This specialized chemical is designed for advanced research and industrial applications, offering exceptional reactivity due to its fluoro and nitrile functional groups. Ideal for pharmaceutical intermediates, agrochemical synthesis, and material science research, this compound is rigorously tested to ensure ??98% purity (GC) and consistency. Supplied in secure, tamper-proof packaging under inert conditions to maintain stability. Suitable for use in cross-coupling reactions, nucleophilic substitutions, and as a building block in heterocyclic chemistry. Store in a cool, dry place away from light and moisture.

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Description

Description

2-Fluoro-5-methylbenzonitrile (CAS No. 64113-84-4) is a high-purity fluorinated aromatic nitrile compound with the molecular formula C8H6FN. This specialized chemical is designed for advanced research and industrial applications, offering exceptional reactivity due to its fluoro and nitrile functional groups. Ideal for pharmaceutical intermediates, agrochemical synthesis, and material science research, this compound is rigorously tested to ensure ??98% purity (GC) and consistency. Supplied in secure, tamper-proof packaging under inert conditions to maintain stability. Suitable for use in cross-coupling reactions, nucleophilic substitutions, and as a building block in heterocyclic chemistry. Store in a cool, dry place away from light and moisture.

  • CAS No: 64113-84-4
  • Molecular Formula: C8H6FN
  • Molecular Weight: 135.14
  • Exact Mass: 135.048427358
  • Monoisotopic Mass: 135.048427358
  • IUPAC Name: 2-fluoro-5-methylbenzonitrile
  • SMILES: CC1=CC(=C(C=C1)F)C#N
  • Synonyms: 2-Fluoro-5-methylbenzonitrile, 64113-84-4, DTXSID90379111, DTXCID00330137, 625-630-9

Application

2-Fluoro-5-methylbenzonitrile serves as a versatile intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals. Its electron-withdrawing nitrile and fluoro groups enhance reactivity in palladium-catalyzed cross-coupling reactions. Researchers utilize this compound to develop novel bioactive molecules and liquid crystal materials. It is also employed in the preparation of fluorinated polymers and advanced organic electronic materials.

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