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CAS 53715-64-3

:

ethyl 4-methyl-2-phenyl-1,3-thiazole-5-carboxylate

Description:
Ethyl 4-methyl-2-phenyl-1,3-thiazole-5-carboxylate, with the CAS number 53715-64-3, is an organic compound characterized by its thiazole ring, which is a five-membered heterocyclic structure containing sulfur and nitrogen. This compound features an ethyl ester functional group, contributing to its solubility in organic solvents. The presence of a phenyl group and a methyl substituent on the thiazole ring enhances its chemical reactivity and may influence its biological activity. Ethyl 4-methyl-2-phenyl-1,3-thiazole-5-carboxylate is typically synthesized through multi-step organic reactions, often involving condensation and esterification processes. It may exhibit various properties such as moderate to high melting and boiling points, depending on the specific conditions and purity. This compound is of interest in medicinal chemistry and material science due to its potential applications in pharmaceuticals and as a building block for more complex molecules. As with many thiazole derivatives, it may also display antimicrobial or anti-inflammatory properties, warranting further investigation into its biological effects.
Formula:C13H13NO2S
InChI:InChI=1/C13H13NO2S/c1-3-16-13(15)11-9(2)14-12(17-11)10-7-5-4-6-8-10/h4-8H,3H2,1-2H3
SMILES:CCOC(=O)c1c(C)nc(c2ccccc2)s1
Synonyms:
  • ETHYL 4-METHYL-2-PHENYL-1,3-THIAZOLE-5-CARBOXYLATE
  • 5-Thiazolecarboxylic acid, 4-methyl-2-phenyl-, ethyl ester
  • BUTTPARK 94\16-01
  • ETHYL 4-METHYL-2-PHENYLTHIAZOLE-5-CARBOXYLATE
  • Ethyl 4-methyl-2-phenyl-1,3-thiazole-5-carboxylate ,97%
  • 4-Methyl-2-phenyl-thiazole-5-carboxylic acid ethyl ester
  • Ethyl 4-methyl-2-phenyl-5-thiazolecarboxylate
  • 5-(Ethoxycarbonyl)-4-methyl-2-phenyl-1,3-thiazole
  • 4-Methyl-2-phenyl-5-thiazolecarboxylicacid,ethylester
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