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CAS 17900-75-3

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2-Chloro-N-[2-(1,1-dimethylethyl)phenyl]acetamide

Description:
2-Chloro-N-[2-(1,1-dimethylethyl)phenyl]acetamide, with the CAS number 17900-75-3, is an organic compound characterized by its amide functional group and the presence of a chloro substituent. This compound features a bulky tert-butyl group attached to a phenyl ring, which influences its steric properties and reactivity. The chloro group introduces a halogen, enhancing the compound's potential for nucleophilic substitution reactions. Typically, compounds of this nature exhibit moderate solubility in organic solvents and may have limited solubility in water due to their hydrophobic characteristics. The presence of the amide group suggests potential for hydrogen bonding, which can affect the compound's boiling and melting points. Additionally, this compound may exhibit biological activity, making it of interest in pharmaceutical research. Its structural features suggest it could interact with various biological targets, although specific biological activities would require empirical investigation. Overall, 2-Chloro-N-[2-(1,1-dimethylethyl)phenyl]acetamide is a compound of interest in both synthetic organic chemistry and medicinal chemistry contexts.
Formula:C12H16ClNO
InChI:InChI=1S/C12H16ClNO/c1-12(2,3)9-6-4-5-7-10(9)14-11(15)8-13/h4-7H,8H2,1-3H3,(H,14,15)
InChI key:InChIKey=GPZNPCANPIZPKU-UHFFFAOYSA-N
SMILES:C(C)(C)(C)C1=C(NC(CCl)=O)C=CC=C1
Synonyms:
  • Acetamide, 2-chloro-N-[2-(1,1-dimethylethyl)phenyl]-
  • 2-Chloro-N-[2-(1,1-dimethylethyl)phenyl]acetamide
  • Acetanilide, 2′-tert-butyl-2-chloro-
  • 2-Chloro-2′-tert-butylacetanilide
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