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Atomfair 6-Bromo-2-methyl-1,3-benzoxazole C8H6BrNO

Description 6-Bromo-2-methyl-1,3-benzoxazole (CAS No. 151230-42-1) is a high-purity heterocyclic organic compound with the molecular formula C8H6BrNO. This brominated benzoxazole derivative features a methyl group at the 2-position, making it a valuable intermediate in pharmaceutical and agrochemical research. With a molecular weight of 212.05 g/mol, it is a white to off-white crystalline solid that is soluble in common organic solvents such as DMSO, methanol, and dichloromethane. Its structural motif is widely utilized in medicinal chemistry for the synthesis of bioactive molecules, particularly in the development of kinase inhibitors and antimicrobial agents. Suitable for laboratory use only, this compound is rigorously tested…

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Description

Description

6-Bromo-2-methyl-1,3-benzoxazole (CAS No. 151230-42-1) is a high-purity heterocyclic organic compound with the molecular formula C8H6BrNO. This brominated benzoxazole derivative features a methyl group at the 2-position, making it a valuable intermediate in pharmaceutical and agrochemical research. With a molecular weight of 212.05 g/mol, it is a white to off-white crystalline solid that is soluble in common organic solvents such as DMSO, methanol, and dichloromethane. Its structural motif is widely utilized in medicinal chemistry for the synthesis of bioactive molecules, particularly in the development of kinase inhibitors and antimicrobial agents. Suitable for laboratory use only, this compound is rigorously tested for purity (typically ??95% by HPLC or GC analysis) and is packaged under inert conditions to ensure stability.

  • CAS No: 151230-42-1
  • Molecular Formula: C8H6BrNO
  • Molecular Weight: 212.04
  • Exact Mass: 210.96328
  • Monoisotopic Mass: 210.96328
  • IUPAC Name: 6-bromo-2-methyl-1,3-benzoxazole
  • SMILES: CC1=NC2=C(O1)C=C(C=C2)Br
  • Synonyms: 6-BROMO-2-METHYL-1,3-BENZOXAZOLE, 802-981-8, 6-Bromo-2-methylbenzo[d]oxazole, 151230-42-1, 6-BROMO-2-METHYLBENZOXAZOLE

Application

6-Bromo-2-methyl-1,3-benzoxazole serves as a key building block in organic synthesis, particularly for constructing benzoxazole-based pharmacophores. It is employed in the development of potential drug candidates targeting inflammatory and infectious diseases. Researchers also utilize this compound in material science for designing fluorescent probes and optoelectronic materials. Its reactivity enables functionalization at the bromine site for cross-coupling reactions, such as Suzuki-Miyaura or Buchwald-Hartwig couplings.

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