675876-25-2

Basic information

• Product Name: but-2-enedioic acid benzyl-{benzylcarbamoyl-[1-(2-nitro-benzenesulfonyl)-1H-pyrrol-2-yl]-methyl}-amide propylamide
• Synonyms: but-2-enedioic acid benzyl-{benzylcarbamoyl-[1-(2-nitro-benzenesulfonyl)-1H-pyrrol-2-yl]-methyl}-amide propylamide
• CAS NO: 675876-25-2
• Molecular Weight: 643.72
• Mol File: 675876-25-2.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: but-2-enedioic acid benzyl-{benzylcarbamoyl-[1-(2-nitro-benzenesulfonyl)-1H-pyrrol-2-yl]-methyl}-amide propylamide(CAS DataBase Reference)
• NIST Chemistry Reference: but-2-enedioic acid benzyl-{benzylcarbamoyl-[1-(2-nitro-benzenesulfonyl)-1H-pyrrol-2-yl]-methyl}-amide propylamide(675876-25-2)
• EPA Substance Registry System: but-2-enedioic acid benzyl-{benzylcarbamoyl-[1-(2-nitro-benzenesulfonyl)-1H-pyrrol-2-yl]-methyl}-amide propylamide(675876-25-2)

Safety Data

• Hazardous Substances Data: 675876-25-2(Hazardous Substances Data)

Upstream product

• 36342-07-1 N-Propyl maleamic acid 
• 88333-03-3 Benzyl isocyanide 
• 1694-92-4 2-Nitrobenzenesulfonyl chloride 
• 54254-38-5 1-(2-nitrophenylsulfonyl)-1H-pyrrole-2-carboxaldehyde 
• 1003-29-8 2-pyrrole aldehyde 

Relevant articles and documents

An Atom-Economical Approach to Conformationally Constrained Tricyclic Nitrogen Heterocycles via Sequential and Tandem Ugi/Intramolecular Diels-Alder Reaction of Pyrrole

An efficient approach to rigid tricyclic nitrogen heterocycles via sequential and tandem Ugi/intramolecular Diels-Alder (IMDA) cycloaddition of pyrrole is described. The one-pot Ugi four-component condensation (4CC) reaction was used as the key transforma