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CAS 4815-29-6

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4H-Cyclopenta[b]thiophene-3-carboxylic acid, 2-amino-5,6-dihydro-, ethyl ester

Description:
4H-Cyclopenta[b]thiophene-3-carboxylic acid, 2-amino-5,6-dihydro-, ethyl ester, with CAS number 4815-29-6, is an organic compound characterized by its unique bicyclic structure that incorporates both a thiophene and cyclopentane moiety. This compound features a carboxylic acid functional group and an ethyl ester, which contribute to its reactivity and solubility properties. The presence of the amino group enhances its potential for hydrogen bonding and may influence its biological activity. Typically, compounds of this nature are of interest in organic synthesis and materials science due to their potential applications in pharmaceuticals, organic electronics, and as intermediates in chemical reactions. The compound's stability, solubility, and reactivity can be influenced by the substituents on the bicyclic framework, making it a subject of study in various chemical contexts. Overall, its structural characteristics suggest it may exhibit interesting electronic properties and biological activities, warranting further investigation in both synthetic and applied chemistry.
Formula:C10H13NO2S
InChI:InChI=1S/C10H13NO2S/c1-2-13-10(12)8-6-4-3-5-7(6)14-9(8)11/h2-5,11H2,1H3
InChI key:InChIKey=BOJXCJDYZJSPMZ-UHFFFAOYSA-N
SMILES:C(OCC)(=O)C=1C2=C(SC1N)CCC2
Synonyms:
  • 4H-Cyclopenta[b]thiophene-3-carboxylic acid, 2-amino-5,6-dihydro-, ethyl ester
  • Ethyl 2-aminocyclopenta[b]thiophene-3-carboxylate
  • NSC 99004
  • ethyl 2-amino-5,6-dihydro-4H-cyclopenta[b]thiophene-3-carboxylate
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