CAS 4793-24-2
:Ácido 5-(aminossulfonil)-2-cloro-4-fluorobenzoico
- 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:Fórmula:C7H5ClFNO4SPureza:98%Cor e Forma:SolidPeso molecular:253.63532-Chloro-4-fluoro-5-sulfamoylbenzoic acid
CAS:2-Chloro-4-fluoro-5-sulfamoylbenzoic acidPureza:95%Peso molecular: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.Fórmula:C7H5ClFNO4SPureza:Min. 95.5 Area-%Cor e Forma:PowderPeso molecular:253.64 g/mol2-Chloro-4-fluoro-5-sulfamoylbenzoic acid
CAS:Fórmula:C7H5ClFNO4SPureza:98%Cor e Forma:SolidPeso molecular:253.632-Chloro-4-fluoro-5-sulfamoylbenzoic Acid
CAS:Produto ControladoApplications 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)Fórmula:C7H5ClFNO4SCor e Forma:NeatPeso molecular: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.
Fórmula:C7H5ClFNO4SPureza:Min. 95%Cor e Forma:PowderPeso molecular:253.64 g/mol





