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Atomfair 3-Nitrobenzoyl bromide C7H4BrNO3

Description 3-Nitrobenzoyl bromide (CAS No. 13277-62-8) is a highly reactive aromatic acyl bromide derivative with the molecular formula C7H4BrNO3. This compound is characterized by a nitro group positioned at the meta position relative to the benzoyl bromide functional group, making it a valuable intermediate in organic synthesis and pharmaceutical research. It is typically supplied as a crystalline solid or solution, with high purity grades (??98%) available for sensitive applications. 3-Nitrobenzoyl bromide is moisture-sensitive and should be stored under inert conditions to prevent hydrolysis. Its reactivity makes it ideal for acylations, peptide coupling, and the synthesis of nitro-substituted aromatic compounds. Suitable…

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Description

Description

3-Nitrobenzoyl bromide (CAS No. 13277-62-8) is a highly reactive aromatic acyl bromide derivative with the molecular formula C7H4BrNO3. This compound is characterized by a nitro group positioned at the meta position relative to the benzoyl bromide functional group, making it a valuable intermediate in organic synthesis and pharmaceutical research. It is typically supplied as a crystalline solid or solution, with high purity grades (??98%) available for sensitive applications. 3-Nitrobenzoyl bromide is moisture-sensitive and should be stored under inert conditions to prevent hydrolysis. Its reactivity makes it ideal for acylations, peptide coupling, and the synthesis of nitro-substituted aromatic compounds. Suitable for use in research laboratories, this product is packaged in amber glass vials or sealed containers to ensure stability.

  • CAS No: 13277-62-8
  • Molecular Formula: C7H4BrNO3
  • Molecular Weight: 230.02
  • Exact Mass: 228.93746
  • Monoisotopic Mass: 228.93746
  • IUPAC Name: 3-nitrobenzoyl bromide
  • SMILES: C1=CC(=CC(=C1)[N+](=O)[O-])C(=O)Br
  • Synonyms: 3-NITROBENZOYL BROMIDE, 13277-62-8, DTXSID40576017, DTXCID90526789, Benzoyl bromide, 3-nitro-

Application

3-Nitrobenzoyl bromide is widely used as a key reagent in organic synthesis, particularly in the preparation of nitro-substituted benzamides and esters. It serves as an acylating agent in peptide chemistry and pharmaceutical intermediate synthesis. Researchers also employ it in the development of dyes, agrochemicals, and specialty polymers requiring nitro-functionalized aromatic backbones.

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