79130-37-3

Basic information

• Product Name: Benzenesulfonamide, N,N'-1,10-decanediylbis[4-methyl-
• CAS NO: 79130-37-3
• Molecular Formula: C24H36N2O4S2
• Molecular Weight: 480.693
• Mol File: 79130-37-3.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzenesulfonamide, N,N'-1,10-decanediylbis[4-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzenesulfonamide, N,N'-1,10-decanediylbis[4-methyl-(79130-37-3)
• EPA Substance Registry System: Benzenesulfonamide, N,N'-1,10-decanediylbis[4-methyl-(79130-37-3)

Safety Data

• Hazardous Substances Data: 79130-37-3(Hazardous Substances Data)

Upstream product

• 646-25-3 diaminodecane 
• 98-59-9 p-toluenesulfonyl chloride 
• 201230-82-2 carbon monoxide 
• 70-55-3 toluene-4-sulfonamide 
• 3710-30-3 1,7-Octadiene 
• 4101-68-2 1,10-dibromodecane 

Downstream Products

• 87338-10-1 1,8-Bis(p-tolylsulfonyl)-1,8-diazacyclooctadecane 
• 87338-15-6 1,13-bis(p-tolylsulfonyl)-1,13-diaza-4,7,10-trioxacyclotricosane 
• 81506-03-8 4,15-bis(p-tolylsulfonyl)-4,15-diazaoctadecane-1,18-diol 
• 130945-22-1 N,N'-di-p-toluenesulfonyl-N,N'-bis<10-(p-toluenesulfonyloxy)decyl>-1,10-decanediamine 
• 130945-18-5 N,N'-bis(10-hydroxydecyl)-N,N'-di-p-toluenesulfonyl-1,10-decanediamine 
• 120615-14-7 N,N'-bis(10-bromodecyl)-N,N'-di-p-toluenesulfonyl-1,10-decanediamine 
• 120590-13-8 1,12,23,34-tetra-p-toluenesulfonyltetraazacyclotetratetracontane 
• 81506-06-1 N,N',4,15-tetrakis(p-tolylsulfonyl)-4,15-diazaoctadecane-1,18-diamine 
• 81522-67-0 4,15-bis(p-tolylsulfonyl)-4,15-diazaoctadecane-1,18-diyl bis(methanesulfonate) 
• 81506-05-0 4,15-bis(p-tolylsulfonyl)-4,15-diazaoctadecane-1,18-diamine 
• 81506-08-3 1,5,9,20,24,28-hexakis(p-tolylsulfonyl)-1,5,9,20,24,28-hexaazacyclooctatriacontane 
• 277760-15-3 N¹,N⁵,N¹⁶,N²⁰-tetra(p-toluenesulfonyl)-1,20-bis(ethylamino)-5,16-diazaeicosane 
• 277760-06-2 N¹,N⁵,N¹⁶,N²⁰-tetra(p-toluenesulfonyl)-1,20-diamino-5,16-diazaeicosane 
• 278807-31-1 C₃₄H₅₄N₄O₆S₂ 

Relevant articles and documents

A novel rhodium-catalyzed domino-hydroformylation-reaction for the synthesis of sulphonamides

An efficient and highly selective method for the synthesis of sulphonamides by a domino hydroformylation-reductive sulphonamidation reaction has been developed. Various olefins and sulphonamides are converted into the desired products in good yields and with excellent selectivities in the presence of a rhodium/Naphos catalyst. This journal is

Synthesis of Large Macrocyclic Tetraaza Compounds with A Methylene Backbone: Cyclo4, (n = 6,7,8,9 and 10). The Formation of 28-, 32-, 36-, 40- and 44-Membered Rings.

A series of macrocyclic tetraamines with 28-, 32-, 36-, 40- and 44-membered rings have been efficiently prepared from the corresponding ditosylamide and monobromoalcohol derivatives in 6 steps via a double condensation reaction.Overall yields were: 41, 41, 46, 29, and 33 percent, respectively, for 1,8,15,22-tetraazacyclooctacontane (11a), 1,9,17,25-tetraazacyclodotriacontane (11b), 1,10,19,28, tetraazacyclohexatriacontane (11c), 1,11,21,31-tetraazacyclotetracontane (11d) and 1,12,23,34-tetraazacyclotetratetracontane (11e).

Anion Receptor Molecules. Chain Length Dependent Selective Binding of Organic and Biological Dicarboxylate Anions by Ditopic Polyammonium Macrocycles

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