1029801-34-0

Basic information

• Product Name: N-(bicyclo[1.1.0]but-1-yl(4-chlorophenyl)methyl)-4-methylbenzenesulfonamide
• Synonyms: N-(bicyclo[1.1.0]but-1-yl(4-chlorophenyl)methyl)-4-methylbenzenesulfonamide
• CAS NO: 1029801-34-0
• Molecular Weight: 347.865
• Mol File: 1029801-34-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: N-(bicyclo[1.1.0]but-1-yl(4-chlorophenyl)methyl)-4-methylbenzenesulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-(bicyclo[1.1.0]but-1-yl(4-chlorophenyl)methyl)-4-methylbenzenesulfonamide(1029801-34-0)
• EPA Substance Registry System: N-(bicyclo[1.1.0]but-1-yl(4-chlorophenyl)methyl)-4-methylbenzenesulfonamide(1029801-34-0)

Safety Data

• Hazardous Substances Data: 1029801-34-0(Hazardous Substances Data)

Upstream product

• 67003-20-7 1,1-dibromo-2-(chloromethyl)cyclopropane 
• 357417-22-2 N-(4-chlorobenzylidene)-4-methylbenzenesulfonamide 

Downstream Products

• 1029801-44-2 N-allyl-N-(bicyclo[1.1.0]but-1-yl(4-chlorophenyl)methyl)-4-methylbenzenesulfonamide 

Relevant articles and documents

Rhodium(I)-catalyzed cycloisomerizations of bicyclobutanes

The selection of rhodium precatalyst and phosphine ligand determines the course of the cycloisomerization of N-allylated bicyclo[1.1.0]butylalkylamines. Cyclopropane-fused pyrrolidines and azepines are obtained with high levels of stereo- and regiocontrol. Novel azatricyclo[6.1.0.01,5]nonanes are the result of a tandem cycloisomerization-ring closing metathesis sequence. Allylic ethers lead to furans and oxepanes. Copyright