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CAS 170355-38-1

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3-Thiophenecarboxylic acid, 5-bromo-, ethyl ester

Description:
3-Thiophenecarboxylic acid, 5-bromo-, ethyl ester is an organic compound characterized by the presence of a thiophene ring, a five-membered aromatic heterocycle containing sulfur. This compound features a carboxylic acid functional group that is esterified with an ethyl group, indicating that it is an ethyl ester. The bromine substituent at the 5-position of the thiophene ring introduces a halogen, which can influence the compound's reactivity and physical properties. Generally, compounds like this exhibit moderate solubility in organic solvents and may have varying degrees of polarity due to the presence of both the thiophene ring and the carboxylic acid moiety. The presence of the bromine atom can also enhance the compound's electrophilic character, making it useful in various chemical reactions, including nucleophilic substitutions. Additionally, such compounds may have applications in pharmaceuticals, agrochemicals, or materials science, depending on their specific reactivity and functional properties. Overall, 3-Thiophenecarboxylic acid, 5-bromo-, ethyl ester is a versatile compound with potential utility in synthetic organic chemistry.
Formula:C7H7BrO2S
InChI:InChI=1/C7H7BrO2S/c1-2-10-7(9)5-3-6(8)11-4-5/h3-4H,2H2,1H3
InChI key:InChIKey=LUYMKCLOYODOEI-UHFFFAOYSA-N
SMILES:C(OCC)(=O)C1=CSC(Br)=C1
Synonyms:
  • 3-Thiophenecarboxylic acid, 5-bromo-, ethyl ester
  • Ethyl 2-bromo-4-thiophenecarboxylate
  • 5-Bromothiophene-3-carboxylic acid ethyl ester
  • Ethyl 5-bromothiophene-3-carboxylate
  • 5-bromo-3-Thiophenecarboxylic acid ethyl ester
  • Ethyl 5-bromothiophene-3-carboxylate 97+%
  • 5-Bromothiophene-3-carboxylic acid ethyl ester, >=98%
  • Ethyl 5-bromothiophene-4-carboxylate
  • PI-35048 ethyl 5-bromothiophene-3-carboxylate
  • 5-BroMo-thiophene-3-carboxylic acid ethyl ester
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