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Atomfair Methyl 2-amino-5-bromo-3-methylbenzoate C9H10BrNO2

Description Methyl 2-amino-5-bromo-3-methylbenzoate (CAS No. 206548-14-3) is a high-purity organic compound with the molecular formula C9H10BrNO2. This aromatic ester features a bromo-substituted benzene ring with an amino and methyl ester functional group, making it a versatile intermediate for pharmaceutical and agrochemical synthesis. Its molecular weight is 244.09 g/mol, and it is characterized by excellent stability under standard laboratory conditions. Ideal for researchers in medicinal chemistry, this compound is supplied with comprehensive analytical data including HPLC, NMR, and MS to ensure quality and consistency. Store in a cool, dry place away from light to maintain integrity.

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Description

Description

Methyl 2-amino-5-bromo-3-methylbenzoate (CAS No. 206548-14-3) is a high-purity organic compound with the molecular formula C9H10BrNO2. This aromatic ester features a bromo-substituted benzene ring with an amino and methyl ester functional group, making it a versatile intermediate for pharmaceutical and agrochemical synthesis. Its molecular weight is 244.09 g/mol, and it is characterized by excellent stability under standard laboratory conditions. Ideal for researchers in medicinal chemistry, this compound is supplied with comprehensive analytical data including HPLC, NMR, and MS to ensure quality and consistency. Store in a cool, dry place away from light to maintain integrity.

  • CAS No: 206548-14-3
  • Molecular Formula: C9H10BrNO2
  • Molecular Weight: 244.08
  • Exact Mass: 242.98949
  • Monoisotopic Mass: 242.98949
  • IUPAC Name: methyl 2-amino-5-bromo-3-methylbenzoate
  • SMILES: CC1=CC(=CC(=C1N)C(=O)OC)Br
  • Synonyms: methyl 2-amino-5-bromo-3-methylbenzoate, 206548-14-3, DTXSID90376943, DTXCID50327971, Methyl 2-amino-5-bromo-3-methylbenzenecarboxylate

Application

Methyl 2-amino-5-bromo-3-methylbenzoate is widely used as a key intermediate in the synthesis of active pharmaceutical ingredients (APIs) and specialty chemicals. Its reactive amino and bromo groups facilitate cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, for constructing complex heterocycles. Researchers also employ it in the development of agrochemicals and dyes due to its robust aromatic framework. This compound is particularly valuable in early-stage drug discovery for modifying lead compounds.

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