1413576-24-5

Basic information

• Product Name: 2,2'-(pentane-1,5-diylbis(benzylazanediyl))bis(N-cyclohexylacetamide)
• Synonyms: 2,2'-(pentane-1,5-diylbis(benzylazanediyl))bis(N-cyclohexylacetamide)
• CAS NO: 1413576-24-5
• Molecular Weight: 560.823
• Mol File: 1413576-24-5.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 2,2'-(pentane-1,5-diylbis(benzylazanediyl))bis(N-cyclohexylacetamide)(CAS DataBase Reference)
• NIST Chemistry Reference: 2,2'-(pentane-1,5-diylbis(benzylazanediyl))bis(N-cyclohexylacetamide)(1413576-24-5)
• EPA Substance Registry System: 2,2'-(pentane-1,5-diylbis(benzylazanediyl))bis(N-cyclohexylacetamide)(1413576-24-5)

Safety Data

• Hazardous Substances Data: 1413576-24-5(Hazardous Substances Data)

Upstream product

• 50-00-0 formaldehyd 
• 931-53-3 Cyclohexyl isocyanide 
• 41640-76-0 N¹,N⁵-dibenzylpentane-1,5-diamine 

Relevant articles and documents

An efficient synthesis of symmetric and unsymmetric bis-(β- aminoamides) via Ugi multicomponent reaction

A library of symmetrical and unsymmetrical bis-(β-aminoamides) has been prepared starting from symmetrical secondary diamines by using a double Ugi four-component reaction. A sacrifical Mumm rearrangement, thanks to the use of 2-hydroxymethyl benzoic acid, is necessary to suppress the competing split-Ugi reaction, increasing the yield and simplifying the purification step. The scope, the reaction conditions, and the role of water in trapping the nitrilium intermediate are also discussed.