102600-39-5

Basic information

• Product Name: Benzenesulfonamide, N,N'-1,4-butanediylbis[N,4-dimethyl-
• Synonyms: Benzenesulfonamide,N,N'-1,4-butanediylbis[N,4-dimethyl;N,N'-Dimethyl-N,N'-butandiyl-bis-toluol-4-sulfonamid;N,4-Dimethyl-N-(4-(methyl[(4-methylphenyl)sulfonyl]amino)butyl)benzenesulfonamide;N,N'-dimethyl-N,N'-butanediyl-bis-toluene-4-sulfonamide;N,N'-Bis[p-tolylsulfonyl]-N,N'-dimethyl-1,4-butanediamine
• CAS NO: 102600-39-5
• Molecular Formula: C20H28N2O4S2
• Molecular Weight: 424.585
• Mol File: 102600-39-5.mol

Chemical Properties

• Boiling Point: 573.2±60.0 °C(Predicted)
• Density: 1.223±0.06 g/cm3(Predicted)
• CAS DataBase Reference: Benzenesulfonamide, N,N'-1,4-butanediylbis[N,4-dimethyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfonamide, N,N'-1,4-butanediylbis[N,4-dimethyl-(102600-39-5)
• EPA Substance Registry System: Benzenesulfonamide, N,N'-1,4-butanediylbis[N,4-dimethyl-(102600-39-5)

Safety Data

• Hazardous Substances Data: 102600-39-5(Hazardous Substances Data)

Upstream product

• 15544-47-5 N,N'-ditosyl-1,4-diaminobutane 
• 77-78-1 dimethyl sulfate 
• 98-59-9 p-toluenesulfonyl chloride 
• 110-52-1 1,4-dibromo-butane 
• 74-88-4 methyl iodide 

Downstream Products

• 16011-97-5 N,N'-dimethyl-1,4-butanediamine 
• 138913-26-5 1,3-dimethyl-1,3-diazacycloheptane 

Relevant articles and documents

Structure-activity relationships of diamines, dicarboxamides, and disulfonamides on vinblastine accumulation in P388/ADR cells

Diamines, dicarboxamides, and disulfonamides that have terminal benzene, methyl- or chloro-substituted benzene rings were synthesized and evaluated for the activity of [3H]vinblastine accumulation in multidrug-resistant P388/ADR cells. The effi

Condensation of Alkanediamines with Formaldehyde; Intramolecular Disproportionation of N-Hydroxymethyl Groups into N-Methyl and N-Formyl Groups

The condensation of α,ω-alkanediamines NH2(CN2)nNH2 with aqueous formaldehyde has been studied by NMR spectroscopy of isolated products and of product mixtures.The condensation was reversible and gave products of widely different types depending on alkane chain length: bicyclic oxadiaza compounds (n = 2, 3, 4), a tricyclic tetraaza compound (n = 2), a quinquecyclic octaaza compound (n = 3), two-dimensional polymers (n = 4, 5).A slow irreversible rearrangement gave in two cases (n = 3, 4), unicyclic 1-formyl-3-methyl-1,3-diaza compounds.The condensation of N,N'-dimethyl-α,ω-alkandediamines CH3NH(CH2)nNHCH3 with aqueous formaldehyde was also studied.The reversible formation of simple unicyclic diaza compounds was observed in all cases (n = 2, 3, 4), but in one case (n = 2) there was again a slow irreversible rearrangement to the N-formyl-N,N'N'-trimethyl derivative.The rearrangement reaction involves a hydride shift and is strictly intramolecular.The conditions for its occurrence can be understood on a conformational basis.