99358-06-2

Basic information

• Product Name: S-nitrophenyl O-ethylxanthate
• Synonyms: S-nitrophenyl O-ethylxanthate
• CAS NO: 99358-06-2
• Molecular Weight: 243.307
• Mol File: 99358-06-2.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: S-nitrophenyl O-ethylxanthate(CAS DataBase Reference)
• NIST Chemistry Reference: S-nitrophenyl O-ethylxanthate(99358-06-2)
• EPA Substance Registry System: S-nitrophenyl O-ethylxanthate(99358-06-2)

Safety Data

• Hazardous Substances Data: 99358-06-2(Hazardous Substances Data)

Upstream product

• 140-89-6 potassium ethyl xanthogenate 
• 586-78-7 para-nitrophenyl bromide 
• 636-98-6 p-nitrobenzene iodide 
• 1849-36-1 para-nitrobenzenethiol 
• 2812-73-9 Chlor(thioameisensaeure)-O-ethylester 
• 100-01-6 4-nitro-aniline 

Downstream Products

• 1849-36-1 para-nitrobenzenethiol 
• 110-85-0 piperazine 
• 5308-12-3 O-ethyl N-(4-methylphenyl)thiocarbamate 
• 3111-89-5 O-ethyl-N-phenylthiocarbamate 
• 64-17-5 ethanol 
• 98-74-8 4-Nitrobenzenesulfonyl chloride 
• 952-97-6 4-nitrophenyl phenyl sulfide 
• 55365-85-0 O-Ethyl N-Butylthiocarbamate 
• 22007-38-1 O-ethyl N-(4-methoxyphenyl)thiocarbamate 
• 936-64-1 morpholinyl thiocarbamate 
• 56525-81-6 1-piperidinecarbothioic acid O-ethyl ester 
• 56525-82-7 1-pyrrolidinecarbothioic acid O-ethyl ester 
• 22001-51-0 O-ethyl N-(4-chlorophenyl)thiocarbamate 

Relevant articles and documents

Copper nanoparticles supported on polyaniline-functionalized multiwall carbon nanotubes: An efficient and recyclable catalyst for synthesis of unsymmetric sulfides using potassium ethyl xanthogenate in water

A new and powerful polyaniline-functionalized carbon nanotube-supported copper(II) nanoparticle catalyst was successfully prepared and evaluated as a heterogeneous catalyst for the one-pot synthesis of unsymmetric thioethers by coupling of aryl, alkyl and benzyl halides using potassium ethyl xanthogenate as source of sulfur in water. All of these reactions gave the desired products in good to excellent yields. The catalyst is available, air-stable and can be reused several times without significant loss in its catalytic activity.

A new effective synthesis of arene mono- and disulfonyl chlorides

Arene mono- and disulfonyl chlorides have been easily synthesized starting from the corresponding anilines via aqueous oxidative chlorination of S-aryl O-ethyl dithiocarbonates intermediates, aryl methyl sulfides, or from arenethiols. Georg Thieme Verlag Stuttgart.