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CAS 351-38-2

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2-Chloro-N-[3-(trifluoromethyl)phenyl]acetamide

Description:
2-Chloro-N-[3-(trifluoromethyl)phenyl]acetamide, with the CAS number 351-38-2, is an organic compound characterized by its amide functional group and the presence of both chlorine and trifluoromethyl substituents. This compound typically appears as a solid at room temperature and is known for its moderate solubility in organic solvents. The presence of the trifluoromethyl group enhances its lipophilicity and can influence its biological activity, making it of interest in pharmaceutical research. The chlorine atom contributes to its reactivity, potentially participating in nucleophilic substitution reactions. The compound's structure suggests it may exhibit specific interactions with biological targets, which can be explored in medicinal chemistry. Additionally, its stability under standard conditions makes it suitable for various applications, including as an intermediate in the synthesis of more complex molecules. Safety data should be consulted for handling, as halogenated compounds can pose environmental and health risks. Overall, 2-Chloro-N-[3-(trifluoromethyl)phenyl]acetamide is a compound of interest in both synthetic and medicinal chemistry contexts.
Formula:C9H7ClF3NO
InChI:InChI=1S/C9H7ClF3NO/c10-5-8(15)14-7-3-1-2-6(4-7)9(11,12)13/h1-4H,5H2,(H,14,15)
InChI key:InChIKey=MOEJRZLPQODXGM-UHFFFAOYSA-N
SMILES:N(C(CCl)=O)C1=CC(C(F)(F)F)=CC=C1
Synonyms:
  • 2-Chloro-N-[3-(trifluoromethyl)phenyl]acetamide
  • m-Acetotoluidide, 2-chloro-α,α,α-trifluoro-
  • 2-Chloro-m-trifluoromethylacetanilide
  • N-(Chloroacetyl)-3-(trifluoromethyl)aniline
  • Acetamide, 2-chloro-N-[3-(trifluoromethyl)phenyl]-
  • N-(3-Trifluoromethylphenyl)-2-chloroacetamide
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