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CAS 175202-26-3

:

3-Chloro-4-[(1-methylethyl)sulfonyl]-2-thiophenecarboxylic acid

Description:
3-Chloro-4-[(1-methylethyl)sulfonyl]-2-thiophenecarboxylic acid is a chemical compound characterized by its thiophene ring structure, which is a five-membered aromatic ring containing sulfur. The presence of a chloro group and a sulfonyl group attached to the thiophene enhances its reactivity and solubility in various solvents. This compound typically exhibits acidic properties due to the carboxylic acid functional group, allowing it to participate in acid-base reactions. Its sulfonyl group contributes to its potential as a leaving group in nucleophilic substitution reactions. The compound may also display biological activity, making it of interest in pharmaceutical research. Its molecular structure suggests it could interact with various biological targets, potentially leading to applications in drug development. Additionally, the presence of the isopropyl group may influence its steric properties and overall reactivity. As with many organic compounds, safety precautions should be taken when handling this substance, including the use of appropriate personal protective equipment.
Formula:C8H9ClO4S2
InChI:InChI=1S/C8H9ClO4S2/c1-4(2)15(12,13)5-3-14-7(6(5)9)8(10)11/h3-4H,1-2H3,(H,10,11)
InChI key:InChIKey=YBTCUNQIEVRDNE-UHFFFAOYSA-N
SMILES:S(C(C)C)(=O)(=O)C=1C(Cl)=C(C(O)=O)SC1
Synonyms:
  • 2-Thiophenecarboxylic acid, 3-chloro-4-[(1-methylethyl)sulfonyl]-
  • 3-Chloro-4 (Isopropylsulfonyl)-2-Carboxylic Acid
  • 3-Chloro-4 (Isopropylsulfonyl)Thiophene-2-Carboxyl
  • 3-Chloro-4-(propane-2-sulfonyl)thiophene-2-carboxylic acid
  • 3-Chloro-4-(propane-2-sulphonyl)-thiophene-2-carboxylic acid
  • 3-Chloro-4-[(1-methylethyl)sulfonyl]-2-thiophenecarboxylic acid
  • 3-Chloro-4-(isopropylsulfonyl)thiophene-2-carboxylic acid
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