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Atomfair 3-Bromoanisole m-Bromoanisole C7H7BrO

Description 3-Bromoanisole (CAS No. 2398-37-0), also known as 1-bromo-3-methoxybenzene or m-Bromoanisole, is a high-purity aromatic bromo compound with the molecular formula C7H7BrO . This organobromine reagent features a methoxy group meta to the bromine substituent, making it a versatile intermediate in synthetic organic chemistry. Available in >98% purity (GC), our 3-Bromoanisole is rigorously tested for consistency, with low levels of non-volatile residues and trace metals. Suitable for Grignard reactions, cross-coupling (e.g., Suzuki, Stille), and electrophilic aromatic substitutions. Packaged under inert gas in amber glass bottles to ensure stability. Technical data includes: MW 187.04 g/mol, density 1.49 g/cm3, boiling point 211-213??C,…

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Description

Description

3-Bromoanisole (CAS No. 2398-37-0), also known as 1-bromo-3-methoxybenzene or m-Bromoanisole, is a high-purity aromatic bromo compound with the molecular formula C7H7BrO. This organobromine reagent features a methoxy group meta to the bromine substituent, making it a versatile intermediate in synthetic organic chemistry. Available in >98% purity (GC), our 3-Bromoanisole is rigorously tested for consistency, with low levels of non-volatile residues and trace metals. Suitable for Grignard reactions, cross-coupling (e.g., Suzuki, Stille), and electrophilic aromatic substitutions. Packaged under inert gas in amber glass bottles to ensure stability. Technical data includes: MW 187.04 g/mol, density 1.49 g/cm3, boiling point 211-213??C, and refractive index n20D 1.562. Store at 2-8??C in a dry environment.

  • CAS No: 2398-37-0
  • Molecular Formula: C7H7BrO
  • Molecular Weight: 187.03
  • Exact Mass: 185.96803
  • Monoisotopic Mass: 185.96803
  • IUPAC Name: 1-bromo-3-methoxybenzene
  • SMILES: COC1=CC(=CC=C1)Br
  • Synonyms: 3-Bromoanisole, 2398-37-0, 1-BROMO-3-METHOXYBENZENE, m-Bromoanisole, 3-Methoxybromobenzene

Application

3-Bromoanisole serves as a key building block in pharmaceutical and agrochemical synthesis, particularly for introducing methoxyphenyl motifs. It is employed in palladium-catalyzed cross-coupling reactions to construct biaryl ethers and complex aromatic systems. Researchers utilize this compound as a precursor for liquid crystals and OLED materials due to its stable aromatic core. The bromine moiety allows further functionalization via halogen-metal exchange or nucleophilic substitution.

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