35735-57-0

Basic information

• Product Name: N,N-diallyl-(4-nitrobenzene)sulfonylamine
• Synonyms: N,N-diallyl-(4-nitrobenzene)sulfonylamine
• CAS NO: 35735-57-0
• Molecular Weight: 282.32
• Mol File: 35735-57-0.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: N,N-diallyl-(4-nitrobenzene)sulfonylamine(CAS DataBase Reference)
• NIST Chemistry Reference: N,N-diallyl-(4-nitrobenzene)sulfonylamine(35735-57-0)
• EPA Substance Registry System: N,N-diallyl-(4-nitrobenzene)sulfonylamine(35735-57-0)

Safety Data

• Hazardous Substances Data: 35735-57-0(Hazardous Substances Data)

Upstream product

• 1104387-60-1 isopropyl N-(4-nitrobenzenesulfonyl)propionimidate 
• 107-18-6 allyl alcohol 
• 98-74-8 4-Nitrobenzenesulfonyl chloride 
• 124-02-7 diallylamine 

Downstream Products

• 18836-83-4 1-[(4-nitrophenyl)sulfonyl]-1H-pyrrole 
• 193891-96-2 N,N-diallyl-4-aminobenzenesulfonamide 

Relevant articles and documents

Synthesis of N -Sulfonyl- and N -Acylpyrroles via a Ring-Closing Metathesis/Dehydrogenation Tandem Reaction

N -Sulfonyl- and N -acylpyrroles were synthesized via olefin ring-closing metathesis of diallylamines and in situ oxidative aromatization in the presence of the ruthenium Grubbs catalyst and a suitable copper catalyst. In the presence of Cu(OTf) 2/s

Mechanochemical ruthenium-catalyzed olefin metathesis

We describe the development of a mechanochemical approach for Ru-catalyzed olefin metathesis, including cross-metathesis and ring-closing metathesis. The method uses commercially available catalysts to achieve high-yielding, rapid, room-temperature metathesis of solid or liquid olefins on a multigram scale using either no or only a catalytic amount of a liquid.