210347-86-7

Basic information

• Product Name: N-benzyl-4-methyl-N-(prop-2-en-1-yl)benzene-1-sulfonamide
• Synonyms: N-benzyl-4-methyl-N-(prop-2-en-1-yl)benzene-1-sulfonamide
• CAS NO: 210347-86-7
• Molecular Weight: 301.409
• Mol File: 210347-86-7.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: N-benzyl-4-methyl-N-(prop-2-en-1-yl)benzene-1-sulfonamide(CAS DataBase Reference)
• NIST Chemistry Reference: N-benzyl-4-methyl-N-(prop-2-en-1-yl)benzene-1-sulfonamide(210347-86-7)
• EPA Substance Registry System: N-benzyl-4-methyl-N-(prop-2-en-1-yl)benzene-1-sulfonamide(210347-86-7)

Safety Data

• Hazardous Substances Data: 210347-86-7(Hazardous Substances Data)

Upstream product

• 1576-37-0 N-benzyl-p-toluenesulfonamide 
• 875312-97-3 N-benzyl-4-methyl-N-(prop-2-yn-1-yl)benzenesulfonamide 
• 172217-57-1 N-benzyl-4-methyl-N-(propa-1,2-dien-1-yl)benzenesulfonamide 
• 100-46-9 benzylamine 
• 98-59-9 p-toluenesulfonyl chloride 
• 4165-79-1 1,1-diphenyl-3-buten-1-ol 
• 70-55-3 toluene-4-sulfonamide 
• 50487-71-3 4-methyl-N-(2-propenyl)benzenesulfonamide 
• 100-39-0 benzyl bromide 

Downstream Products

• 1207251-41-9 C₂₁H₂₈NO₅PS 
• 700336-74-9 (E)-N-benzyl-4-methyl-N-(prop-1-en-1-yl)benzenesulfonamide 
• 6271-12-1 N-benzyl-N-propyl-toluene-4-sulfonamide 
• 1576-37-0 N-benzyl-p-toluenesulfonamide 

Relevant articles and documents

Ligand-Controlled Regiodivergence for Catalytic Stereoselective Semireduction of Allenamides

Ligand-controlled regiodivergence has been developed for catalytic semireduction of allenamides with excellent chemo- and stereocontrol. This system also provides an example of catalytic regiodivergent semireduction of allenes for the first time. The divergence of the semireduction is enabled by ligand switch with the same palladium pre-catalyst under operationally simple and mild conditions. Monodentate ligand XPhos exclusively promotes selective 1,2-semireduction to afford allylic amides, while bidentate ligand BINAP completely switched the regioselectivity to 2,3-semireduction, producing (E)-enamide derivatives.

Electrochemical Vicinal Difluorination of Alkenes: Scalable and Amenable to Electron-Rich Substrates

Fluorinated alkyl groups are important motifs in bioactive compounds, positively influencing pharmacokinetics, potency and conformation. The oxidative difluorination of alkenes represents an important strategy for their preparation, yet current methods are limited in their alkene-types and tolerance of electron-rich, readily oxidized functionalities, as well as in their safety and scalability. Herein, we report a method for the difluorination of a number of unactivated alkene-types that is tolerant of electron-rich functionality, giving products that are otherwise unattainable. Key to success is the electrochemical generation of a hypervalent iodine mediator using an “ex-cell” approach, which avoids oxidative substrate decomposition. The more sustainable conditions give good to excellent yields in up to decagram scales.

Tert-Butyl Nitrite: Organic Redox Cocatalyst for Aerobic Aldehyde-Selective Wacker-Tsuji Oxidation

An aldehyde-selective aerobic Wacker-Tsuji oxidation is developed. Using tert-butyl nitrite as a simple organic redox cocatalyst instead of copper or silver salts, a variety of aldehydes were achieved as major products in up to 30/1 regioselectivity as well as good to high yields at room temperature.