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Atomfair 4-Bromo-2-chlorobenzonitrile C7H3BrClN

Description 4-Bromo-2-chlorobenzonitrile (CAS No. 154607-01-9) is a high-purity halogenated benzonitrile derivative with the molecular formula C7H3BrClN . This aromatic nitrile compound is a versatile intermediate in organic synthesis, particularly in pharmaceutical and agrochemical research. Its unique structure, featuring both bromo and chloro substituents on the benzene ring, makes it a valuable precursor for cross-coupling reactions such as Suzuki-Miyaura and Buchwald-Hartwig reactions. The compound is supplied as a crystalline solid with ??98% purity (HPLC), ensuring consistency in research applications. Proper storage at 2-8??C in a tightly sealed container is recommended to maintain stability. Suitable for use under inert conditions due to…

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Description

Description

4-Bromo-2-chlorobenzonitrile (CAS No. 154607-01-9) is a high-purity halogenated benzonitrile derivative with the molecular formula C7H3BrClN. This aromatic nitrile compound is a versatile intermediate in organic synthesis, particularly in pharmaceutical and agrochemical research. Its unique structure, featuring both bromo and chloro substituents on the benzene ring, makes it a valuable precursor for cross-coupling reactions such as Suzuki-Miyaura and Buchwald-Hartwig reactions. The compound is supplied as a crystalline solid with ??98% purity (HPLC), ensuring consistency in research applications. Proper storage at 2-8??C in a tightly sealed container is recommended to maintain stability. Suitable for use under inert conditions due to sensitivity to moisture and air. Handle with appropriate personal protective equipment (PPE) in a fume hood.

  • CAS No: 154607-01-9
  • Molecular Formula: C7H3BrClN
  • Molecular Weight: 216.46
  • Exact Mass: 214.91374
  • Monoisotopic Mass: 214.91374
  • IUPAC Name: 4-bromo-2-chlorobenzonitrile
  • SMILES: C1=CC(=C(C=C1Br)Cl)C#N
  • Synonyms: 4-Bromo-2-chlorobenzonitrile, 154607-01-9, DTXSID10426651, EC 679-039-6, DTXCID40377485

Application

4-Bromo-2-chlorobenzonitrile serves as a key building block in medicinal chemistry for the synthesis of biologically active molecules. It is particularly useful in the development of pharmaceutical candidates through palladium-catalyzed coupling reactions. Researchers utilize this compound to create novel heterocyclic systems in drug discovery programs. The bromo and chloro substituents allow for sequential functionalization, enabling structure-activity relationship (SAR) studies.

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