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CAS 315683-17-1

:

ethyl 2-amino-4-[4-(propan-2-yl)phenyl]thiophene-3-carboxylate

Description:
Ethyl 2-amino-4-[4-(propan-2-yl)phenyl]thiophene-3-carboxylate, with the CAS number 315683-17-1, is a chemical compound characterized by its complex structure, which includes a thiophene ring, an ethyl ester group, and an amino group. This compound features a branched alkyl substituent (isopropyl) on a phenyl ring, contributing to its hydrophobic characteristics. The presence of the amino group suggests potential for hydrogen bonding, which may influence its solubility and reactivity. The thiophene moiety is known for its electronic properties, making this compound potentially interesting for applications in organic electronics or as a building block in pharmaceuticals. Its carboxylate functionality may also enhance its reactivity in various chemical reactions, such as esterification or amidation. Overall, the unique combination of functional groups in this compound suggests diverse applications in medicinal chemistry and materials science, although specific biological activities or industrial uses would require further investigation.
Formula:C16H19NO2S
InChI:InChI=1/C16H19NO2S/c1-4-19-16(18)14-13(9-20-15(14)17)12-7-5-11(6-8-12)10(2)3/h5-10H,4,17H2,1-3H3
SMILES:CCOC(=O)c1c(csc1N)c1ccc(cc1)C(C)C
Synonyms:
  • 3-Thiophenecarboxylic acid, 2-amino-4-[4-(1-methylethyl)phenyl]-, ethyl ester
  • Ethyl 2-amino-4-(4-isopropylphenyl)thiophene-3-carboxylate
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