497949-70-9

Upstream product

• 1189-71-5 isocyanate de chlorosulfonyle 
• 62-53-3 aniline 
• 100-51-6 benzyl alcohol 
• 15959-53-2 N-(1-phenyl)sulfamide 
• 501-53-1 benzyl chloroformate 

Downstream Products

• 41876-52-2 2-benzyl-4-bromoanisole 
• 611-45-0 1-Benzyl-naphthalene 
• 613-59-2 2-benzylnaphthalene 
• 120-32-1 chlorophene 
• 7700-27-8 4-chlorophenyl benzyl ether 
• 101-81-5 Diphenylmethane 
• 4453-79-6 2-benzyl-1,3,5-trimethylbenzene 
• 144446-67-3 (2,4,6-trimethyl-1,3-phenylene)bis(methylene)-dibenzene 
• 16886-10-5 3-benzyl-1H-indole 

Relevant academic research and scientific papers

A Simple, efficient, Catalyst-Free and Solvent-Less Microwave-Assisted process for N-Cbz Protection of Several amines

A simple, green and chemo-selective method for the N-benzyloxycarbonylation of amines, β-amino alcohols, α-amino esters and sulfonamides has been developed under microwave irradiation. Good to excellent yields of the N-benzyloxy-carbamates compounds were obtained in short times without any side products.

Uncatalyzed Friedel-Crafts alkylation of aromatic compounds through reactive benzyl cations generated from N-sulfamoylcarbamates

(Matrix presented) A new method for the generation of highly reactive benzyl cations by thermal decomposition of aryl-benzyl-sulfamoylcarbamates, obtained in a one-pot reaction from chlorosulfonyl isocyanate, is described. The generated cations alkylate aromatic compounds efficiently in the absence of catalysts.