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CAS 160982-10-5

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3-Acetyl-5-chloro-2-thiophenesulfonamide

Description:
3-Acetyl-5-chloro-2-thiophenesulfonamide is a chemical compound characterized by its unique structure, which includes a thiophene ring, an acetyl group, and a sulfonamide functional group. The presence of the chlorine atom at the 5-position of the thiophene ring contributes to its reactivity and potential biological activity. This compound is typically a solid at room temperature and may exhibit moderate solubility in polar solvents due to the sulfonamide group, which can engage in hydrogen bonding. Its sulfonamide moiety suggests potential applications in medicinal chemistry, particularly as an antibacterial or antifungal agent, as many sulfonamides are known for their therapeutic properties. The acetyl group may also influence the compound's lipophilicity and overall pharmacokinetic profile. Additionally, the compound's synthesis and stability can be influenced by the presence of the chlorine atom and the thiophene ring, making it an interesting subject for further research in organic and medicinal chemistry.
Formula:C6H6ClNO3S2
InChI:InChI=1S/C6H6ClNO3S2/c1-3(9)4-2-5(7)12-6(4)13(8,10)11/h2H,1H3,(H2,8,10,11)
InChI key:InChIKey=ODLFFSHLXVZFPY-UHFFFAOYSA-N
SMILES:C(C)(=O)C1=C(S(N)(=O)=O)SC(Cl)=C1
Synonyms:
  • 2-Thiophenesulfonamide, 3-Acetyl-5-Chloro-
  • 3-Acetyl-5-chloro-2-thiophenesulfonamide
  • 3-Acetyl-5-chlorothiophene-2-sulfonamide
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