934421-18-8

Basic information

• Product Name: N-(cyclohexylcarbamoyl-furan-2-yl-methyl)-N-(2-hydroxy-ethyl)-3-(toluene-4-sulfonylamino)-propionamide
• Synonyms: N-(cyclohexylcarbamoyl-furan-2-yl-methyl)-N-(2-hydroxy-ethyl)-3-(toluene-4-sulfonylamino)-propionamide
• CAS NO: 934421-18-8
• Molecular Weight: 491.609
• Mol File: 934421-18-8.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-(cyclohexylcarbamoyl-furan-2-yl-methyl)-N-(2-hydroxy-ethyl)-3-(toluene-4-sulfonylamino)-propionamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(cyclohexylcarbamoyl-furan-2-yl-methyl)-N-(2-hydroxy-ethyl)-3-(toluene-4-sulfonylamino)-propionamide(934421-18-8)
• EPA Substance Registry System: N-(cyclohexylcarbamoyl-furan-2-yl-methyl)-N-(2-hydroxy-ethyl)-3-(toluene-4-sulfonylamino)-propionamide(934421-18-8)

Safety Data

• Hazardous Substances Data: 934421-18-8(Hazardous Substances Data)

Upstream product

• 931-53-3 Cyclohexyl isocyanide 
• 42908-33-8 3-{[(4-methylphenyl)sulfonyl]amino}propanoic acid 
• 10530-89-9 2-ethanol 
• 98-01-1 furfural 

Relevant articles and documents

Ugi multicomponent reaction followed by an intramolecular nucleophilic substitution: Convergent multicomponent synthesis of 1-sulfonyl 1,4-diazepan-5-ones and of their benzo-fused derivatives

A short, two-step approach to the synthesis of diazepane or diazocane systems, based on a Ugi multicomponent reaction followed by a subsequent intramolecular SN2 reaction was studied. 1 -Sulfonyl tetrahydrobenzo[e]-1,4-diazepin-1-ones 1 were ob