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CAS 2564-02-5

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N-(4-Bromophenyl)-2-chloroacetamide

Description:
N-(4-Bromophenyl)-2-chloroacetamide is an organic compound characterized by its amide functional group, which is derived from the reaction of 4-bromobenzoic acid and chloroacetyl chloride. This compound features a bromine atom attached to a phenyl ring, contributing to its unique chemical properties, including potential reactivity and biological activity. The presence of the chloroacetamide moiety suggests that it may exhibit polar characteristics, influencing its solubility in various solvents. It is typically a solid at room temperature and may have applications in pharmaceuticals or as an intermediate in organic synthesis. The compound's molecular structure allows for potential interactions with biological targets, making it of interest in medicinal chemistry. Safety data should be consulted, as halogenated compounds can pose health risks, and appropriate handling procedures should be followed. Overall, N-(4-Bromophenyl)-2-chloroacetamide is a noteworthy compound in the realm of organic chemistry, with implications for both research and application.
Formula:C8H7BrClNO
InChI:InChI=1S/C8H7BrClNO/c9-6-1-3-7(4-2-6)11-8(12)5-10/h1-4H,5H2,(H,11,12)
InChI key:InChIKey=FRZKCMCCQAJIBN-UHFFFAOYSA-N
SMILES:N(C(CCl)=O)C1=CC=C(Br)C=C1
Synonyms:
  • 2-Chloro-4′-bromoacetanilide
  • 2-Chloro-N-(4-bromophenyl)acetamide
  • 2-Chloro-N-(p-bromophenyl)acetamide
  • Acetamide, N-(4-bromophenyl)-2-chloro-
  • Acetanilide, 4′-bromo-2-chloro-
  • N-(4-Bromophenyl)-2-Chloroacetamide
  • N-(4-Bromophenyl)chloroacetamide
  • N-(Chloroacetyl)-4-bromoaniline
  • N-Chloroacetyl-p-bromoaniline
  • NSC 220248
  • p-Bromo-2-chloroacetanilide
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