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CAS 306934-99-6

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ethyl 2-amino-4-(4-bromophenyl)thiophene-3-carboxylate

Description:
Ethyl 2-amino-4-(4-bromophenyl)thiophene-3-carboxylate is a chemical compound characterized by its unique structure, which includes a thiophene ring, an amino group, and a carboxylate ester. The presence of the bromophenyl group enhances its potential for various applications in medicinal chemistry and organic synthesis. This compound typically exhibits moderate solubility in organic solvents, reflecting its aromatic and heterocyclic nature. Its molecular structure suggests potential reactivity, particularly in electrophilic substitution reactions due to the electron-withdrawing effects of the bromine atom. The amino group can participate in hydrogen bonding, influencing its interactions in biological systems. Additionally, the ethyl ester moiety may undergo hydrolysis under certain conditions, leading to the corresponding carboxylic acid. Overall, ethyl 2-amino-4-(4-bromophenyl)thiophene-3-carboxylate is of interest for its potential biological activity and utility in the development of pharmaceuticals or agrochemicals.
Formula:C13H12BrNO2S
InChI:InChI=1/C13H12BrNO2S/c1-2-17-13(16)11-10(7-18-12(11)15)8-3-5-9(14)6-4-8/h3-7H,2,15H2,1H3
InChI key:InChIKey=SEWFWRCESBYGFS-UHFFFAOYSA-N
SMILES:C(OCC)(=O)C=1C(=CSC1N)C2=CC=C(Br)C=C2
Synonyms:
  • 2-Amino-4-(4-bromophenyl)thiophene-3-carboxylic acid ethyl ester
  • 3-Thiophenecarboxylic acid, 2-amino-4-(4-bromophenyl)-, ethyl ester
  • Ethyl 2-amino-4-(4-bromophenyl)thiophene-3-carboxylate
  • Ethyl 2-amino-4-(4-bromophenyl)-3-thiophenecarboxylate ,98%
  • AKOS MSC-0438
  • TIMTEC-BB SBB005954
  • AKOS B000791
  • 2-AMINO-4-(4-BROMO-PHENYL)-THIOPHENE-3-CARBOXYLIC ACID ETHYL ESTER
  • ETHYL 2-AMINO-4-(4-BROMOPHENYL)-3-THIOPHENECARBOXYLATE
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