93624-01-2

Basic information

• Product Name: O-ethyl S-2-(4-methoxyphenyl)-2-oxoethyl carbonodithioate
• Synonyms: O-ethyl S-2-(4-methoxyphenyl)-2-oxoethyl carbonodithioate
• CAS NO: 93624-01-2
• Molecular Weight: 270.373
• Mol File: 93624-01-2.mol
• Article Data: 9

Chemical Properties

• CAS DataBase Reference: O-ethyl S-2-(4-methoxyphenyl)-2-oxoethyl carbonodithioate(CAS DataBase Reference)
• NIST Chemistry Reference: O-ethyl S-2-(4-methoxyphenyl)-2-oxoethyl carbonodithioate(93624-01-2)
• EPA Substance Registry System: O-ethyl S-2-(4-methoxyphenyl)-2-oxoethyl carbonodithioate(93624-01-2)

Safety Data

• Hazardous Substances Data: 93624-01-2(Hazardous Substances Data)

Upstream product

• 140-89-6 potassium ethyl xanthogenate 
• 2632-13-5 2-Bromo-4'-methoxyacetophenone 
• 140-90-9 sodium O-ethyl dithiocarbonate 
• 6832-17-3 2-diazo-1-(4-methoxyphenyl)ethanone 
• 186581-53-3 diazomethane 
• 100-09-4 4-methoxybenzoic acid 

Downstream Products

• 226920-50-9 dithiocarbonic acid S-[1-(1-tert-butoxycarbonylamino-1-methyl-ethyl)-4-(4-methoxy-phenyl)-4-oxo-butyl] ester O-ethyl ester 
• 478800-91-8 dithiocarbonic acid O-ethyl ester S-{1-[3-(4-methoxy-phenyl)-3-oxo-propyl]-heptyl} ester 
• 517867-34-4 2,2-dimethylpropionic acid 1-ethoxythiocarbonylsulfanyl-4-(4-methoxyphenyl)-4-oxobutyl ester 
• 100-06-1 1-(4-methoxyphenyl)ethanone 
• 1164111-69-6 (E)-4-(4-chloro-phenyl)-7-(4-methoxy-phenyl)-7-oxo-hept-2-enoic acid ethyl ester 
• 1370229-49-4 5-(6-hydroxy-3-methoxyphenyl)piperidin-2-one 
• 1370229-44-9 dithiocarbonic acid S-[1-((tert-butoxycarbonylamino)methyl)-4-(4-methoxyphenyl)-4-oxobutyl] ester O-ethyl ester 
• 42545-43-7 2-(4-methoxyphenyl)thiophene 
• 15982-64-6 1,4-bis(4-methoxyphenyl)butane-1,4-dione 
• 88559-25-5 4-(4-Methoxybenzoyl)-5-methylthio-1,3-dithiol-2-thion 

Relevant articles and documents

α-Xanthylmethyl Ketones from α-Diazo ketones

A simple and efficient method to obtain α-xanthylmethyl ketones from α-diazo ketones is described. The reaction proceeds through a protonation/nucleophilic substitution sequence in the presence of p -toluenesulfonic acid and potassium ethyl xanthogenate as the nucleophile. As α-diazo ketones can be readily synthesized from ubiquitous carboxylic acids, a broad variety of xanthates can be obtained, including examples from naturally occurring substrates.

Synthesis of pyrazolylvinyl ketones from furan derivatives

A new protocol for the synthesis of pyrazol-5-ylvinyl ketones, e.g. pyrazole-chalcones, employing furfuryl ketones as a triketone equivalent, has been developed. The reaction occurs under mild conditions and does not require the use of expensive materials

Flexible routes to thiophenes

Three convergent routes to thiophenes are described, hinging on the radical addition of α-xanthyl ketones to ethyl vinyl sulfide or to vinyl pivalate. The latter route ultimately proved to be the most versatile and efficient (61-94%).