28371-57-5

Basic information

• Product Name: (4-nitrophenyl)methyl diethyldithiocarbamate
• Synonyms: (4-nitrophenyl)methyl diethyldithiocarbamate
• CAS NO: 28371-57-5
• Molecular Weight: 284.403
• Mol File: 28371-57-5.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: (4-nitrophenyl)methyl diethyldithiocarbamate(CAS DataBase Reference)
• NIST Chemistry Reference: (4-nitrophenyl)methyl diethyldithiocarbamate(28371-57-5)
• EPA Substance Registry System: (4-nitrophenyl)methyl diethyldithiocarbamate(28371-57-5)

Safety Data

• Hazardous Substances Data: 28371-57-5(Hazardous Substances Data)

Upstream product

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

Relevant articles and documents

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.

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.

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.