Atomfair 1-Bromo-4-fluoronaphthalene C10H6BrF

Description 1-Bromo-4-fluoronaphthalene (CAS No. 341-41-3) is a high-purity halogenated naphthalene derivative with the molecular formula C10H6BrF . This aromatic compound is characterized by its bromine and fluorine substituents at the 1- and 4-positions of the naphthalene ring, respectively, making it a valuable intermediate in organic synthesis and materials science. With a molecular weight of 225.06 g/mol, it is a crystalline solid at room temperature, offering excellent stability under standard laboratory conditions. Ideal for researchers in pharmaceuticals, agrochemicals, and advanced material development, our product is rigorously tested to ensure ??98% purity (GC) and is supplied in sealed, light-resistant containers to maintain…

Description

1-Bromo-4-fluoronaphthalene (CAS No. 341-41-3) is a high-purity halogenated naphthalene derivative with the molecular formula C₁₀H₆BrF. This aromatic compound is characterized by its bromine and fluorine substituents at the 1- and 4-positions of the naphthalene ring, respectively, making it a valuable intermediate in organic synthesis and materials science. With a molecular weight of 225.06 g/mol, it is a crystalline solid at room temperature, offering excellent stability under standard laboratory conditions. Ideal for researchers in pharmaceuticals, agrochemicals, and advanced material development, our product is rigorously tested to ensure ??98% purity (GC) and is supplied in sealed, light-resistant containers to maintain integrity. Suitable for Suzuki couplings, nucleophilic substitutions, and as a building block for liquid crystals or OLED materials.

CAS No: 341-41-3
Molecular Formula: C10H6BrF
Molecular Weight: 225.06
Exact Mass: 223.96369
Monoisotopic Mass: 223.96369
IUPAC Name: 1-bromo-4-fluoronaphthalene
SMILES: C1=CC=C2C(=C1)C(=CC=C2Br)F
Synonyms: 1-Bromo-4-fluoronaphthalene, 341-41-3, 1-fluoro-4-bromonaphthalene, EINECS 206-434-9, Naphthalene, 1-bromo-4-fluoro-

Application

1-Bromo-4-fluoronaphthalene is widely used as a key precursor in cross-coupling reactions (e.g., Suzuki-Miyaura) to synthesize biaryl compounds for pharmaceutical and material applications. Its halogenated structure enables facile functionalization in the development of liquid crystals, organic semiconductors, and fluorescent dyes. Researchers also employ it as a model substrate in mechanistic studies of aromatic substitution reactions.

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