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CAS 138098-81-4

:

2-(2-CHLORO-ACETYLAMINO)-4-P-TOLYL-THIOPHENE-3-CARBOXYLIC ACID ETHYL ESTER

Description:
2-(2-Chloro-acetylamino)-4-p-tolyl-thiophene-3-carboxylic acid ethyl ester, identified by its CAS number 138098-81-4, is a chemical compound that features a thiophene ring, which is a five-membered aromatic heterocycle containing sulfur. This compound is characterized by the presence of a chloroacetylamino group and an ethyl ester functional group, contributing to its reactivity and potential applications in organic synthesis. The p-tolyl group indicates the presence of a para-substituted toluene moiety, which can influence the compound's electronic properties and solubility. The carboxylic acid functionality, in the form of an ethyl ester, suggests that it may participate in esterification reactions or hydrolysis under appropriate conditions. This compound may exhibit biological activity, making it of interest in pharmaceutical research. Its specific characteristics, such as melting point, solubility, and spectral data, would typically be determined through experimental methods and are essential for understanding its behavior in various chemical environments.
Formula:C16H16ClNO3S
InChI:InChI=1/C16H16ClNO3S/c1-3-21-16(20)14-12(11-6-4-10(2)5-7-11)9-22-15(14)18-13(19)8-17/h4-7,9H,3,8H2,1-2H3,(H,18,19)
SMILES:CCOC(=O)c1c(csc1N=C(CCl)O)c1ccc(C)cc1
Synonyms:
  • Timtec-Bb Sbb009373
  • 3-Thiophenecarboxylic Acid, 2-[(2-Chloroacetyl)Amino]-4-(4-Methylphenyl)-, Ethyl Ester
  • Akos Au36-M217
  • Akos B015594
  • Ethyl 2-[(2-Chloroacetyl)Amino]-4-(4-Methylphenyl)-3-Thiophenecarboxylate
  • Art-Chem-Bb B015594
  • Ethyl 2-[(Chloroacetyl)Amino]-4-(4-Methylphenyl)Thiophene-3-Carboxylate
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