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Atomfair 5-Bromo-o-toluidine C7H8BrN

Description 5-Bromo-o-toluidine (CAS No. 39478-78-9), also known as 5-bromo-2-methylaniline , is a high-purity aromatic amine compound with the molecular formula C7H8BrN . This fine chemical is widely utilized in organic synthesis, pharmaceutical research, and agrochemical development due to its reactive bromine and amine functional groups. Its crystalline form and consistent purity (>98%) make it ideal for precise laboratory applications, including coupling reactions and heterocyclic synthesis. Packaged under inert conditions to ensure stability, this product is rigorously tested via GC-MS and HPLC to meet stringent quality standards. Suitable for researchers requiring reliable intermediates in medicinal chemistry and material science.

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Description

Description

5-Bromo-o-toluidine (CAS No. 39478-78-9), also known as 5-bromo-2-methylaniline, is a high-purity aromatic amine compound with the molecular formula C7H8BrN. This fine chemical is widely utilized in organic synthesis, pharmaceutical research, and agrochemical development due to its reactive bromine and amine functional groups. Its crystalline form and consistent purity (>98%) make it ideal for precise laboratory applications, including coupling reactions and heterocyclic synthesis. Packaged under inert conditions to ensure stability, this product is rigorously tested via GC-MS and HPLC to meet stringent quality standards. Suitable for researchers requiring reliable intermediates in medicinal chemistry and material science.

  • CAS No: 39478-78-9
  • Molecular Formula: C7H8BrN
  • Molecular Weight: 186.05
  • Exact Mass: 184.98401
  • Monoisotopic Mass: 184.98401
  • IUPAC Name: 5-bromo-2-methylaniline
  • SMILES: CC1=C(C=C(C=C1)Br)N
  • Synonyms: 39478-78-9, 5-Bromo-o-toluidine, EINECS 254-467-2, DTXSID00192616, DTXCID40115107

Application

5-Bromo-o-toluidine serves as a key intermediate in the synthesis of dyes, pharmaceuticals, and agrochemicals. Its bromine substituent enables electrophilic aromatic substitution reactions, while the amine group facilitates diazotization for azo dye production. Researchers also employ it in palladium-catalyzed cross-coupling reactions to construct complex organic frameworks.

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