100330-20-9

Upstream product

• 2917-26-2 16-mercaptohexadecanoate 
• 100-44-7 benzyl chloride 
• 4860-03-1 1-Chlorohexadecan 
• 100-53-8 phenylmethanethiol 
• 112-82-3 hexadecanyl bromide 
• 100-39-0 benzyl bromide 
• 66143-73-5 n-cetyl thiocyanate 

Downstream Products

• 4860-03-1 1-Chlorohexadecan 
• 831-91-4 Benzyl phenyl sulfide 
• 37616-35-6 hexadecyl-phenyl sulfide 
• 100-44-7 benzyl chloride 
• 100339-90-0 3,3,6-Trimethyl-4-phenylmercapto-heptadien-(1,5) 
• 7110-00-1 n-hexadecyl benzyl sulfoxide 

Relevant academic research and scientific papers

A simple and efficient method for preparation of unsymmetrical sulfides

A simple and high efficient method for preparation of unsymmetrical sulfides is described.

A novel one pot synthesis of benzyl sulfides: Samarium-induced, benzyl bromide mediated reduction of alkyl thiocyanates and diaryl disulfides in methanol

A convenient synthesis of benzyl Sulfides by the treatment of alkyl thiocyanates or diaryl disulfides with metallic samarium and benzyl bromide in methanol has been developed.

Chemoselective alkylation of thiols: A detailed investigation of reactions of thiols with halides

Arylthiols, aralkylthiols and alkane thiols can be readily alkylated by alkyl/aralkyl halides in presence of K2CO3/DMF to yield unsymmetrical sulphides in nearly quantitative yields. 2-Mercaptoethanol gave the thioether chemoselectively.