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Atomfair 1-Fluoronaphthalene C10H7F

Description 1-Fluoronaphthalene (CAS No. 321-38-0) is a high-purity fluorinated aromatic compound with the molecular formula C10H7F , widely utilized in organic synthesis and material science research. This colorless to pale-yellow liquid exhibits excellent thermal stability and is commonly employed as a solvent, intermediate, or building block in the preparation of advanced materials, pharmaceuticals, and agrochemicals. With a boiling point of approximately 215??C and a melting point of -13??C , it is suitable for high-temperature reactions. Our product is rigorously tested to ensure ??98% purity (GC) and is available in various packaging options under inert gas to maintain integrity. Ideal for…

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Description

Description

1-Fluoronaphthalene (CAS No. 321-38-0) is a high-purity fluorinated aromatic compound with the molecular formula C10H7F, widely utilized in organic synthesis and material science research. This colorless to pale-yellow liquid exhibits excellent thermal stability and is commonly employed as a solvent, intermediate, or building block in the preparation of advanced materials, pharmaceuticals, and agrochemicals. With a boiling point of approximately 215??C and a melting point of -13??C, it is suitable for high-temperature reactions. Our product is rigorously tested to ensure ??98% purity (GC) and is available in various packaging options under inert gas to maintain integrity. Ideal for researchers requiring precise fluorination chemistry or studying naphthalene derivatives.

  • CAS No: 321-38-0
  • Molecular Formula: C10H7F
  • Molecular Weight: 146.16
  • Exact Mass: 146.053178385
  • Monoisotopic Mass: 146.053178385
  • IUPAC Name: 1-fluoronaphthalene
  • SMILES: C1=CC=C2C(=C1)C=CC=C2F
  • Synonyms: 1-FLUORONAPHTHALENE, Naphthalene, 1-fluoro-, alpha-Fluoronaphthalene, 1-Fluornaftalen, .alpha.-Fluoronaphthalene

Application

1-Fluoronaphthalene serves as a versatile fluorinated precursor in organic synthesis, particularly for Suzuki-Miyaura cross-coupling reactions to create biaryl compounds. It is also used as a solvent in NMR spectroscopy due to its distinct 19F signal. In materials science, it acts as a monomer for fluorinated polymers with enhanced thermal and chemical resistance.

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