29128-01-6

Basic information

• Product Name: Benzene, 1-[(1,3-diphenyl-2-propenyl)sulfonyl]-4-methyl-
• CAS NO: 29128-01-6
• Molecular Formula: C22H20O2S
• Molecular Weight: 348.466
• Mol File: 29128-01-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: Benzene, 1-[(1,3-diphenyl-2-propenyl)sulfonyl]-4-methyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1-[(1,3-diphenyl-2-propenyl)sulfonyl]-4-methyl-(29128-01-6)
• EPA Substance Registry System: Benzene, 1-[(1,3-diphenyl-2-propenyl)sulfonyl]-4-methyl-(29128-01-6)

Safety Data

• Hazardous Substances Data: 29128-01-6(Hazardous Substances Data)

Upstream product

• 33866-99-8 2-(1,3-diphenylallyl)hydrazide-p-toluenesulfonic acid 
• 1576-35-8 toluene-4-sulfonic acid hydrazide 
• 73930-97-9 3-acetoxy-1,3-diphenylpropene 
• 824-79-3 sodium 4-methylbenzenesulfinate 
• 10439-23-3 4-methylbenzenesulfinyl chloride 
• 4663-33-6 1,3-diphenyl-3-hydroxypropene 
• 29128-04-9 α-Acetoxy-1,3-diphenylpropan-2-on-p-toluolsulfonylhydrazon 
• 66551-92-6 1-acetoxy-1,3-diphenyl-acetone 
• 29127-97-7 2-Tosylazo-1,3-diphenylpropen 
• 536-57-2 p-toluene sulfinic acid 

Relevant articles and documents

Palladium-catalyzed aerobic oxidative coupling of enantioenriched primary allylic amines with sulfonyl hydrazides leading to optically active allylic sulfones

A range of highly enantioenriched primary allylic amines underwent palladium-catalyzed oxidative coupling with sulfonyl hydrazides open to air at room temperature to give structurally diverse allylic sulfones in moderate to excellent yields with excellent retention of ee. This journal is the Partner Organisations 2014.

Palladium catalyzed asymmetric sulfonylation mediated chiral β-hydroxy- and β-(o-diphenylphosphino)benzoyloxy (o-diphenyl phosphino)benzamides

The palladium catalyzed asymmetric allylic sulfonylation reaction has been investigated employing β-hydroxy- and β-(o-diphenylphosphino) benzoyloxy (o-diphenyl phosphino)benzamides as chiral, non-racemic ligands. The bisphosphine β-benzoyloxybenzamide ligands proved to be the best ligands for this process. Competitive transition states for the (1S,2R)-norephedrine derived ligand 14 are compared and a rationale is provided for the observed enantioselectivities.