28371-57-5

Upstream product

• 28535-08-2 methylene bis-(di-ethylamino-dithioformate) 
• 98-95-3 nitrobenzene 
• 75-15-0 carbon disulfide 
• 109-89-7 diethylamine 
• 100-11-8 1-bromomethyl-4-nitro-benzene 
• 99-99-0 1-methyl-4-nitrobenzene 
• 97-77-8 disulfiram 
• 147-84-2 Diethyldithiocarbamic acid 
• 100-14-1 4-nitrobenzyl chloride 
• 619-73-8 4-nitrobenzyl chloride 

Relevant academic research and scientific papers

Magnetic nanocrystals coated by molecularly imprinted polymers for the recognition of bisphenol A

Molecularly imprinted polymers were coated on the surface of magnetic nanoparticles using an original and simple chemical strategy combining aryl diazonium salt chemistry and the iniferter method. This approach provides dispersed, highly soluble and BPA imprinted poly(methacrylic acid-co-ethylene glycoldimethacrylate) coated magnetic nanoparticles.

Transition-Metal-Free C(sp3)–S Coupling in Water: Synthesis of Benzyl Dithiocarbamates Using Thiuram Disulfides as an Organosulfur Source

A simple, highly efficient and environmentally benign method for the synthesis of benzyl dithiocarbamates was reported. Without addition of metal catalyst, a series of 34 benzyl dithiocarbamates were obtained in good to excellent yields by treating benzyl halides with tetraalkylthiuram disulfides in water. The protocol allows easy access to C(sp3)–S bond formation, features the advantages of easy performance, environmental friendliness, good to excellent yields, and good functional tolerance, showing potential value for the preparation of some biologically active compounds.

Direct conversion of methylarenes into dithiocarbamates, thioamides and benzyl esters

A new strategy for the synthesis of a variety of dithiocarbamates and thioamides has been developed employing inexpensive and readily available methylarenes under metal-free and solvent-free conditions. The approach offers a one-pot procedure and has also been extended to the synthesis of a diverse range of benzyl esters.

Straightforward and highly efficient catalyst-free one-pot synthesis of dithiocarbamates under solvent-free conditions

A highly efficient and simple synthesis of dithiocarbamates is possible based on the one-pot reaction of amines, CS2, and alkyl halides without using a catalyst under solvent-free conditions. The mild reaction conditions, high yields, and broad scope of the reaction illustrate the good synthetic utility of this method. The reaction is a highly atom-economic process for production of S-alkyl thiocarbamates and successfully can be used in high quantities in the pharmaceutical or agrochemical industries.

A one-pot rapid synthesis of dithiocarbamates from alcohols using a polymer supported diethyl dithiocarbamate anion

A polymer supported diethyl dithiocarbamate anion reacts with primary and secondary alcohols via their tirfluoracetates giving alkylated diethyl dithiocarbamates in good yields.