CAS 4793-24-2
:Acide 5-(aminosulfonyl)-2-chloro-4-fluorobenzoïque
- 5-Aminosulfonyl-2-chloro-4-fluorobenzoic acid
- 2-Chloro-4-fluoro-5-sulfamoylbenzoic acid
- 5-(Aminosulfonyl)-2-chloro-4-fluorobenzoic acid
- Benzoic acid, 2-chloro-4-fluoro-5-sulfamoyl-
- Benzoic acid, 5-(aminosulfonyl)-2-chloro-4-fluoro-
2-Chloro-4-fluoro-5-sulfamoylbenzoic acid
CAS :Formule :C7H5ClFNO4SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :253.63532-Chloro-4-fluoro-5-sulfamoylbenzoic acid
CAS :2-Chloro-4-fluoro-5-sulfamoylbenzoic acidDegré de pureté :95%Masse moléculaire :253.64g/mol2-Chloro-4-fluoro-5-sulfamoylbenzoic acid
CAS :2-Chloro-4-fluoro-5-sulfamoylbenzoic acid is a sulfonamide-based compound with potential antibacterial activity to inhibit folic acid synthesis, an essential process for bacterial growth and reproduction. Additionally, the presence of the sulfamoyl group may contribute to diuretic properties, making it a candidate for treating conditions like hypertension and edema. Furthermore, this compound could exhibit antidiabetic effects by inhibiting carbonic anhydrase enzymes involved in glucose metabolism and insulin secretion, although further research is necessary to validate these applications.Formule :C7H5ClFNO4SDegré de pureté :Min. 95.5 Area-%Couleur et forme :PowderMasse moléculaire :253.64 g/mol2-Chloro-4-fluoro-5-sulfamoylbenzoic acid
CAS :Formule :C7H5ClFNO4SDegré de pureté :98%Couleur et forme :SolidMasse moléculaire :253.632-Chloro-4-fluoro-5-sulfamoylbenzoic Acid
CAS :Produit contrôléApplications 2-Chloro-4-fluoro-5-sulfamoylbenzoic Acid is used as a reagent in the synthesis of N-benzyl-N'-(4-piperidinyl)urea CCR5 antagonists as anti-HIV-1 agents.
References Duan, M., et al.: Bioorg. Med. Chem. Lett., 20, 7401 (2010)Formule :C7H5ClFNO4SCouleur et forme :NeatMasse moléculaire :253.642-Chloro-4-fluoro-5-sulfamoylbenzoic acid - Bio-X ™
CAS :2-Chloro-4-fluoro-5-sulfamoylbenzoic acid is a sulfonamide-based compound with potential antibacterial activity to inhibit folic acid synthesis, an essential process for bacterial growth and reproduction. Additionally, the presence of the sulfamoyl group may contribute to diuretic properties, making it a candidate for treating conditions like hypertension and edema. Furthermore, this compound could exhibit antidiabetic effects by inhibiting carbonic anhydrase enzymes involved in glucose metabolism and insulin secretion, although further research is necessary to validate these applications.
Formule :C7H5ClFNO4SDegré de pureté :Min. 95%Couleur et forme :PowderMasse moléculaire :253.64 g/mol





