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CAS 36050-35-8

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5-methyl-4-nitrothiophene-2-carboxylic acid

Description:
5-Methyl-4-nitrothiophene-2-carboxylic acid is an organic compound characterized by its thiophene ring structure, which is a five-membered aromatic heterocycle containing sulfur. The presence of a methyl group and a nitro group at specific positions on the thiophene ring contributes to its unique chemical properties. The carboxylic acid functional group (-COOH) enhances its acidity and solubility in polar solvents, making it useful in various chemical reactions and applications. This compound typically exhibits moderate stability under standard conditions but may undergo reactions such as nitration, reduction, or esterification depending on the functional groups present. Its nitro group can participate in electrophilic aromatic substitution reactions, while the carboxylic acid can engage in acid-base reactions. Additionally, the compound may exhibit biological activity, making it of interest in pharmaceutical research. Overall, 5-methyl-4-nitrothiophene-2-carboxylic acid is a versatile compound with potential applications in organic synthesis and medicinal chemistry.
Formula:C6H5NO4S
InChI:InChI=1/C6H5NO4S/c1-3-4(7(10)11)2-5(12-3)6(8)9/h2H,1H3,(H,8,9)
SMILES:Cc1c(cc(C(=O)O)s1)N(=O)=O
Synonyms:
  • 2-Thiophenecarboxylic acid, 5-methyl-4-nitro-
  • 5-Methyl-4-nitrothiophene-2-carboxylic acid
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