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CAS 77261-21-3

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Ethyl 2-[(2-chloroacetyl)amino]-4-phenyl-3-thiophenecarboxylate

Description:
Ethyl 2-[(2-chloroacetyl)amino]-4-phenyl-3-thiophenecarboxylate, identified by its CAS number 77261-21-3, is a chemical compound that features a complex structure comprising an ethyl ester, an amide, and a thiophene ring. This compound typically exhibits characteristics common to esters and amides, such as moderate solubility in organic solvents and potential reactivity due to the presence of the chloroacetyl group, which can participate in nucleophilic substitution reactions. The thiophene moiety contributes to its aromatic properties, potentially influencing its electronic characteristics and reactivity. The presence of the phenyl group may enhance its stability and hydrophobicity. This compound may be of interest in medicinal chemistry, particularly for its potential biological activities, which could include antimicrobial or anti-inflammatory properties, although specific biological data would need to be referenced from relevant studies. Overall, its unique structural features suggest a range of possible applications in pharmaceuticals or organic synthesis.
Formula:C15H14ClNO3S
InChI:InChI=1S/C15H14ClNO3S/c1-2-20-15(19)13-11(10-6-4-3-5-7-10)9-21-14(13)17-12(18)8-16/h3-7,9H,2,8H2,1H3,(H,17,18)
InChI key:InChIKey=IWUYJPUGLVYKIK-UHFFFAOYSA-N
SMILES:C(OCC)(=O)C=1C(=CSC1NC(CCl)=O)C2=CC=CC=C2
Synonyms:
  • 2-(2-Chloro-acetylamino)-4-phenyl-thiophene-3-carboxylic acid ethyl ester
  • 2-[(2-Chloroacetyl)amino]-4-phenyl-3-thiophenecarboxylic acid, ethyl ester
  • 3-Thiophenecarboxylic acid, 2-[(2-chloroacetyl)amino]-4-phenyl-, ethyl ester
  • 3-Thiophenecarboxylic acid, 2-[(chloroacetyl)amino]-4-phenyl-, ethyl ester
  • Ethyl 2-[(2-chloroacetyl)amino]-4-phenyl-3-thiophenecarboxylate
  • T5Sj Bmv1G Cvo2 Dr [Wln]
  • Ethyl 2-[(chloroacetyl)amino]-4-phenylthiophene-3-carboxylate
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