59639-96-2

Usage

Uses

Used in Organic Synthesis:
N-Allyl methanesulfonamide is used as a building block for the creation of various other compounds due to its unique properties and strong nucleophilicity.
Used in Pharmaceutical Industry:
N-Allyl methanesulfonamide is used as a precursor in the development of new drugs, leveraging its potential applications in the synthesis of biologically active molecules for medicinal purposes.

Upstream product

• 145429-75-0 N-allyl-N-benzylmethanesulfonamide 

Downstream Products

• 342793-40-2 N-[2-iodo-1-(4-methoxyphenyl)ethyl]-N-(methylsulfonyl)prop-2-enylamine 
• 1011486-82-0 C₁₅H₁₇IN₂O₄S 
• 1227797-14-9 N-(3-(4-acetylphenyl)propyl)methanesulfonamide 
• 1309862-01-8 N-allyl-N-(phenylethynyl)methanesulfonamide 
• 1638755-19-7 N-allyl-N-((2-(methoxy(phenyl)methyl)phenyl)ethynyl)methanesulfonamide 
• 1638755-28-8 N-allyl-N-((4-fluoro-2-(methoxy(phenyl)methyl)phenyl)ethynyl)methanesulfonamide 
• 1638755-31-3 N-allyl-N-((2-((allyloxy)(phenyl)methyl)phenyl)ethynyl)methanesulfonamide 
• 1638755-34-6 N-((2-(methoxy(naphthalen-1-yl)methyl)phenyl)ethynyl)-4-methyl-Nphenylbenzenesulfonamide 

Relevant academic research and scientific papers

Metal-free reductive cleavage of C-N and S-N bonds by photoactivated electron transfer from a neutral organic donor

A photoactivated neutral organic super electron donor cleaves challenging arenesulfonamides derived from dialkylamines at room temperature. It also cleaves a)ArC-NR and b)ArN-C bonds. This study also highlights the assistance given to these cleavage reactions by the groups attached to N in (a) and to C in (b), by lowering LUMO energies and by stabilizing the products of fragmentation. Radical fragmentations: Electron transfer from the photoactivated neutral electron donor 1 delivers high yields of S-N and C-N cleavage products for a range of nitrogen-containing species. These reactions proceed at room temperature and under mild reaction conditions in the absence of any metal reagents. DMF=N,N-dimethylformamide, Ts=4-toluenesulfonyl.