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CAS 953092-76-7

:

methyl 5-chloro-3-hydroxythiophene-2-carboxylate

Description:
Methyl 5-chloro-3-hydroxythiophene-2-carboxylate is an organic compound characterized by its thiophene ring, which is a five-membered aromatic heterocycle containing sulfur. The presence of a chlorine atom at the 5-position and a hydroxyl group at the 3-position contributes to its reactivity and potential applications in various chemical reactions. The carboxylate group, derived from the carboxylic acid, indicates that this compound can participate in esterification and other nucleophilic substitution reactions. This compound may exhibit biological activity, making it of interest in medicinal chemistry and agrochemicals. Its solubility properties are influenced by the functional groups present, which can affect its interactions in biological systems and its utility in synthesis. Additionally, the compound's structure suggests potential for further derivatization, allowing for the exploration of its derivatives in research and development. Overall, methyl 5-chloro-3-hydroxythiophene-2-carboxylate is a versatile compound with significant implications in organic synthesis and potential applications in pharmaceuticals.
Formula:C6H5ClO3S
InChI:InChI=1/C6H5ClO3S/c1-10-6(9)5-3(8)2-4(7)11-5/h2,8H,1H3
SMILES:COC(=O)c1c(cc(Cl)s1)O
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