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Atomfair 1-Bromo-3-(methoxymethyl)benzene C8H9BrO

Description 1-Bromo-3-(methoxymethyl)benzene (CAS No. 1515-89-5) is a high-purity aromatic compound with the molecular formula C8H9BrO . This specialized chemical is characterized by its bromine substitution and methoxymethyl functional group, making it a versatile intermediate in organic synthesis and pharmaceutical research. It is supplied as a clear to pale-yellow liquid with a molecular weight of 201.06 g/mol and a boiling point of approximately 230-232??C. Ideal for researchers and scientists, our product undergoes rigorous QC testing (including GC/MS and NMR) to ensure ??98% purity. Suitable for use in Suzuki couplings, Grignard reactions, and as a building block for advanced materials. Packaged in…

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Description

Description

1-Bromo-3-(methoxymethyl)benzene (CAS No. 1515-89-5) is a high-purity aromatic compound with the molecular formula C8H9BrO. This specialized chemical is characterized by its bromine substitution and methoxymethyl functional group, making it a versatile intermediate in organic synthesis and pharmaceutical research. It is supplied as a clear to pale-yellow liquid with a molecular weight of 201.06 g/mol and a boiling point of approximately 230-232??C. Ideal for researchers and scientists, our product undergoes rigorous QC testing (including GC/MS and NMR) to ensure ??98% purity. Suitable for use in Suzuki couplings, Grignard reactions, and as a building block for advanced materials. Packaged in amber glass bottles under inert gas to ensure stability.

  • CAS No: 1515-89-5
  • Molecular Formula: C8H9BrO
  • Molecular Weight: 201.06
  • Exact Mass: 199.98368
  • Monoisotopic Mass: 199.98368
  • IUPAC Name: 1-bromo-3-(methoxymethyl)benzene
  • SMILES: COCC1=CC(=CC=C1)Br
  • Synonyms: 1-BROMO-3-(METHOXYMETHYL)BENZENE, 1515-89-5, 3-bromobenzyl methyl ether, DTXSID80529300, DTXCID40480089

Application

1-Bromo-3-(methoxymethyl)benzene is widely used as a key intermediate in pharmaceutical synthesis, particularly for the development of active pharmaceutical ingredients (APIs) and agrochemicals. Its reactive bromine moiety enables cross-coupling reactions (e.g., Suzuki-Miyaura) to construct biaryl structures. The methoxymethyl group serves as a protective group or functional handle in medicinal chemistry. Researchers also utilize this compound in material science for designing liquid crystals and organic electronic materials.

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