Description

4-Methyl-N-[[[3-[[(4-methylphenyl)sulfonyl]oxy]phenyl]amino]carbonyl]benzenesulfonamide (CAS No. 232938-43-1) is a high-purity sulfonamide derivative with the molecular formula C₂₁H₂₀N₂O₆S₂. This compound features a unique molecular structure incorporating dual sulfonamide functionalities, making it a valuable intermediate for organic synthesis and pharmaceutical research. With a precise IUPAC name of [3-[(4-methylphenyl)sulfonylcarbamoylamino]phenyl] 4-methylbenzenesulfonate, it is characterized by its high stability and reactivity in controlled conditions. Ideal for researchers in medicinal chemistry, this compound is supplied with comprehensive analytical data including HPLC, NMR, and MS to ensure quality and consistency. Store in a cool, dry environment away from light to maintain integrity.

Properties

• CAS Number: 232938-43-1
• Complexity: 802
• IUPAC Name: [3-(p-tolylsulfonylcarbamoylamino)phenyl] 4-methylbenzenesulfonate
• InChI: InChI=1S/C21H20N2O6S2/c1-15-6-10-19(11-7-15)30(25,26)23-21(24)22-17-4-3-5-18(14-17)29-31(27,28)20-12-8-16(2)9-13-20/h3-14H,1-2H3,(H2,22,23,24)
• InChI Key: HEVGMYPGMWZOBU-UHFFFAOYSA-N
• Exact Mass: 460.07627871
• Molecular Formula: C21H20N2O6S2
• Molecular Weight: 460.5
• SMILES: CC1=CC=C(C=C1)S(=O)(=O)NC(=O)NC2=CC(=CC=C2)OS(=O)(=O)C3=CC=C(C=C3)C
• Topological: 135
• Monoisotopic Mass: 460.07627871
• Synonyms: 4-Methyl-N-[[[3-[[(4-methylphenyl)sulfonyl]oxy]phenyl]amino]carbonyl]benzenesulfonamide, Benzenesulfonamide, 4-methyl-N-(((3-(((4-methylphenyl)sulfonyl)oxy)phenyl)amino)carbonyl)-, 4-Methyl-N-(((3-(((4-methylphenyl)sulfonyl)oxy)phenyl)amino)carbonyl)benzenesulfonamide, BENZENESULFONAMIDE, 4-METHYL-N-[[[3-[[(4-METHYLPHENYL)SULFONYL]OXY]PHENYL]AMINO]CARBONYL]-, 232938-43-1, Pergafast201, 3-(3-Tosylureido)phenyl p-toluenesulfonate, Pergafast 201, 3-(3-Tosylureido)phenyl 4-methylbenzenesulfonate, [3-[(4-methylphenyl)sulfonylcarbamoylamino]phenyl] 4-methylbenzenesulfonate, EC 432-520-2, 3-((((4-Methylphenyl)sulfonyl)carbamoyl)amino)phenyl 4-methylbenzenesulfonate, SCHEMBL27367, DTXSID90872910, HEVGMYPGMWZOBU-UHFFFAOYSA-N, Benzenesulfonamide,4-methyl-N-[[[3-[[(4-methylphenyl)sulfonyl]oxy]phenyl]amino]carbonyl]-, NS00004605, G69977, N-(p-Toluolsulfonyl)-N’-(3-(p-toluolsulfonyloxy)phenyl)harnstoff, 4-Methyl-N-[[[3-[[(4-methylphenyl)sulfonyl]oxi]phenyl]amino]carbonyl]-benzensulfonamide

Application

This compound serves as a versatile building block in the synthesis of sulfonamide-based pharmaceuticals, particularly in the development of enzyme inhibitors and receptor modulators. Its dual sulfonyl groups make it suitable for cross-coupling reactions and as a precursor in heterocyclic chemistry. Researchers may also explore its potential in designing novel antimicrobial or anti-inflammatory agents due to its structural resemblance to bioactive sulfonamides.

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