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CAS 70374-37-7

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5-Chloro-3-(N-methylsulfamoyl)-thiophene-2-carboxylic acid methyl ester

Description:
5-Chloro-3-(N-methylsulfamoyl)-thiophene-2-carboxylic acid methyl ester is a chemical compound characterized by its thiophene ring structure, which is a five-membered aromatic heterocycle containing sulfur. The presence of a chloro substituent at the 5-position and a methylsulfamoyl group at the 3-position contributes to its unique reactivity and potential applications in medicinal chemistry. The carboxylic acid methyl ester functionality indicates that it can undergo hydrolysis to yield the corresponding carboxylic acid, which may enhance its solubility and reactivity in various chemical environments. This compound is likely to exhibit polar characteristics due to the presence of the sulfonamide group, which can engage in hydrogen bonding. Its structural features suggest potential biological activity, making it of interest in pharmaceutical research. Additionally, the compound's stability and reactivity can be influenced by the electronic effects of the chloro and methylsulfamoyl groups, which may affect its interactions with biological targets or other chemical species.
Formula:C7H8ClNO4S2
InChI:InChI=1/C7H8ClNO4S2/c1-9-15(11,12)4-3-5(8)14-6(4)7(10)13-2/h3,9H,1-2H3
SMILES:CNS(=O)(=O)c1cc(Cl)sc1C(=O)OC
Synonyms:
  • Methyl 5-chloro-N-(methoxycarbony lmethyl)-3-sulfamoylthiophene-2-carboxylate
  • 5-Cl-TCMC
  • Methyl 5-Chloro-3-(Methylsulfamoyl)Thiophene-2-Carboxylate
  • 5-Chloro-3-(Methylamino)Sulfamoyl-2-Carboxylic Acid Methyl Ester
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