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CAS 175276-54-7

:

Ethyl 4-formyl-2,5-dimethyl-1-(2-thienylmethyl)-1H-pyrrole-3-carboxylate

Description:
Ethyl 4-formyl-2,5-dimethyl-1-(2-thienylmethyl)-1H-pyrrole-3-carboxylate, with the CAS number 175276-54-7, is a chemical compound characterized by its complex structure, which includes a pyrrole ring, a formyl group, and an ethyl ester functional group. This compound features a thienylmethyl substituent, contributing to its unique reactivity and potential applications in organic synthesis and medicinal chemistry. The presence of multiple methyl groups and the ethyl ester enhances its lipophilicity, which may influence its biological activity and solubility in organic solvents. The pyrrole ring is known for its aromatic properties, which can impart stability and influence the electronic characteristics of the molecule. Additionally, the formyl group can participate in various chemical reactions, such as condensation and reduction, making this compound a versatile intermediate in synthetic pathways. Overall, its structural features suggest potential utility in the development of pharmaceuticals or agrochemicals, although specific applications would depend on further research and exploration of its properties.
Formula:C15H17NO3S
InChI:InChI=1S/C15H17NO3S/c1-4-19-15(18)14-11(3)16(10(2)13(14)9-17)8-12-6-5-7-20-12/h5-7,9H,4,8H2,1-3H3
InChI key:InChIKey=XGNWYRXJIRVWGK-UHFFFAOYSA-N
SMILES:C(OCC)(=O)C=1C(C=O)=C(C)N(CC2=CC=CS2)C1C
Synonyms:
  • 1H-Pyrrole-3-carboxylic acid, 4-formyl-2,5-dimethyl-1-(2-thienylmethyl)-, ethyl ester
  • Buttpark 97\57-25
  • Ethyl 2,5-Dimethyl-4-Formyl-1-(Thien-2-Yl)Pyrrole-3-Carboxylate
  • ethyl 4-formyl-2,5-dimethyl-1-(thiophen-2-ylmethyl)-1H-pyrrole-3-carboxylate
  • Ethyl 4-formyl-2,5-dimethyl-1-(2-thienylmethyl)-1H-pyrrole-3-carboxylate
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