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CAS 96232-71-2

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2-Thiophenecarboxylic acid, 4,5-dibromo-3-hydroxy-, methyl ester

Description:
2-Thiophenecarboxylic acid, 4,5-dibromo-3-hydroxy-, methyl ester, with CAS number 96232-71-2, is an organic compound characterized by its thiophene ring structure, which is a five-membered aromatic heterocycle containing sulfur. This compound features a carboxylic acid functional group that is esterified with methanol, resulting in a methyl ester. The presence of bromine substituents at the 4 and 5 positions of the thiophene ring introduces significant electronegative character, which can influence the compound's reactivity and stability. Additionally, the hydroxyl group at the 3 position contributes to its potential for hydrogen bonding, affecting its solubility and interaction with other molecules. This compound may exhibit biological activity due to its structural features, making it of interest in pharmaceutical and agrochemical research. Its physical properties, such as melting point, boiling point, and solubility, would typically be determined through experimental methods, as they can vary based on purity and environmental conditions.
Formula:C6H4Br2O3S
InChI:InChI=1S/C6H4Br2O3S/c1-11-6(10)4-3(9)2(7)5(8)12-4/h9H,1H3
InChI key:InChIKey=BRIPHJFDXWRHAV-UHFFFAOYSA-N
SMILES:C(OC)(=O)C1=C(O)C(Br)=C(Br)S1
Synonyms:
  • Methyl 4,5-dibromo-3-hydroxy-2-thiophenecarboxylate
  • 4,5-Dibromo-3-hydroxy-2-(methoxycarbonyl)thiophene
  • 2-Thiophenecarboxylic acid, 4,5-dibromo-3-hydroxy-, methyl ester
  • 4,5-Dibromo-3-hydroxythiophene-2-carboxylic acid methyl ester
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