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Atomfair Methyl 4-Bromo-3-(bromomethyl)benzoate C9H8Br2O2

Description Methyl 4-Bromo-3-(bromomethyl)benzoate (CAS No. 142031-67-2) is a high-purity brominated aromatic ester with the molecular formula C9H8Br2O2. This compound is a versatile intermediate in organic synthesis, particularly in the preparation of pharmaceuticals, agrochemicals, and specialty materials. Its structure features both a bromomethyl and a bromo substituent on a benzoate ring, enabling selective functionalization for cross-coupling reactions, nucleophilic substitutions, and polymer modifications. Ideal for researchers and industrial chemists, our product is rigorously tested for purity and consistency, ensuring reliable performance in demanding applications. Available in various quantities with detailed analytical data (GC/HPLC, NMR) upon request.

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Description

Description

Methyl 4-Bromo-3-(bromomethyl)benzoate (CAS No. 142031-67-2) is a high-purity brominated aromatic ester with the molecular formula C9H8Br2O2. This compound is a versatile intermediate in organic synthesis, particularly in the preparation of pharmaceuticals, agrochemicals, and specialty materials. Its structure features both a bromomethyl and a bromo substituent on a benzoate ring, enabling selective functionalization for cross-coupling reactions, nucleophilic substitutions, and polymer modifications. Ideal for researchers and industrial chemists, our product is rigorously tested for purity and consistency, ensuring reliable performance in demanding applications. Available in various quantities with detailed analytical data (GC/HPLC, NMR) upon request.

  • CAS No: 142031-67-2
  • Molecular Formula: C9H8Br2O2
  • Molecular Weight: 307.97
  • Exact Mass: 307.88706
  • Monoisotopic Mass: 305.88910
  • IUPAC Name: methyl 4-bromo-3-(bromomethyl)benzoate
  • SMILES: COC(=O)C1=CC(=C(C=C1)Br)CBr
  • Synonyms: Methyl 4-bromo-3-(bromomethyl)benzoate, 142031-67-2, DTXSID00466667, DTXCID90417486, 813-169-8

Application

Methyl 4-Bromo-3-(bromomethyl)benzoate serves as a key building block in medicinal chemistry for the synthesis of bioactive molecules and drug candidates. It is also employed in material science for modifying polymers and creating flame-retardant additives. Its dual bromine functionality allows for sequential derivatization in multi-step synthetic routes.

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