CAS 160982-10-5: 3-Acetyl-5-chloro-2-thiophenesulfonamide
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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Found 5 products.
3-Acetyl-5-chlorothiophene-2-sulfonamide
CAS:Purity:95.0%Color and Shape:SolidMolecular weight:239.690002441406252-Thiophenesulfonamide, 3-acetyl-5-chloro-
CAS:Formula:C6H6ClNO3S2Purity:97%Color and Shape:SolidMolecular weight:239.69973-Acetyl-2-(aminosulfonyl)-5-chlorothiophene
CAS:Formula:C6H6ClNO3S2Purity:>98.0%(T)(HPLC)Color and Shape:White to Light yellow powder to crystalMolecular weight:239.693-Acetyl-2-(aminosulfonyl)-5-chlorothiophene
CAS:3-Acetyl-2-(aminosulfonyl)-5-chlorothiophene is a ketone that was synthesized to inhibit the enzyme carbonic anhydrase. 3-Acetyl-2-(aminosulfonyl)-5-chlorothiophene has been shown to be enantioselective, which means it is more active against one form of the enzyme than another. It is also brominated and has a thioether group. This compound inhibits carbonic anhydrase by binding to the active site of the enzyme, preventing the formation of carbonic acid from bicarbonate and hydrogen ions. 3-Acetyl-2-(aminosulfonyl)-5-chlorothiophene has been shown in research studies to be a chloride ionizable and hydroxylamine alkylation inhibitor. It also has bromohydrin and tosylation properties, as well as anti-inflammatory activities.Formula:C6H6ClNO3S2Purity:Min. 95%Molecular weight:239.7 g/molRef: 3D-FA75881
Discontinued product3-Acetyl-2-(Aminosulfonyl)-5-Chlorothiophene
CAS:3-Acetyl-2-(Aminosulfonyl)-5-ChlorothiophenePurity:98%+Molecular weight:239.70g/mol
