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CAS 2153-08-4

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2-chloro-N-(4-ethoxyphenyl)acetamide

Description:
2-Chloro-N-(4-ethoxyphenyl)acetamide, with the CAS number 2153-08-4, is an organic compound characterized by its amide functional group and the presence of a chloro substituent. This compound features a chloro group attached to the second carbon of the acetamide structure, while the nitrogen atom is bonded to a 4-ethoxyphenyl group, which contributes to its overall hydrophobic character. The ethoxy group enhances the compound's solubility in organic solvents. Typically, compounds of this nature exhibit moderate to low toxicity and may possess biological activity, making them of interest in pharmaceutical research. The presence of the chloro substituent can influence the compound's reactivity and stability, potentially affecting its interactions in biological systems. Additionally, the molecular structure suggests that it may participate in hydrogen bonding due to the amide group, which can impact its physical properties such as melting point and boiling point. Overall, 2-chloro-N-(4-ethoxyphenyl)acetamide is a compound of interest in various chemical and biological applications.
Formula:C10H12ClNO2
InChI:InChI=1S/C10H12ClNO2/c1-2-14-9-5-3-8(4-6-9)12-10(13)7-11/h3-6H,2,7H2,1H3,(H,12,13)
InChI key:InChIKey=NKPPVEIJXVVHGF-UHFFFAOYSA-N
SMILES:CCOc1ccc(cc1)NC(=O)CCl
Synonyms:
  • 2-Chloro-4′-ethoxyacetanilide
  • Acetamide, 2-chloro-N-(4-ethoxyphenyl)-
  • N-Chloroacetyl-4-ethoxyaniline
  • NSC 46900
  • p-Acetophenetidide, 2-chloro-
  • α-Chloro-p-ethoxyacetanilide
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