13037-20-2

Usage

InChI:InChI=1/C9H11NS2/c1-2-12-9(11)10-8-6-4-3-5-7-8/h3-7H,2H2,1H3,(H,10,11)

Upstream product

• 103-72-0 phenyl isothiocyanate 
• 75-08-1 ethanethiol 
• 19801-30-0 S-ethyl-N,N'-diphenyl-isothiourea 
• 62-53-3 aniline 
• 75-03-6 ethyl iodide 
• 74-96-4 ethyl bromide 
• 43009-16-1 phenyldithiocarbamic acid triethylamine salt 

Downstream Products

• 1010-53-3 3-phenyl-2,4-thiazolidinedione 
• 61522-19-8 5-ethoxycarbonyl-2-ethylsulfanyl-4-oxo-3-phenyl-4,5-dihydro-thiazolium betaine 
• 103-72-0 phenyl isothiocyanate 
• 75-08-1 ethanethiol 
• 91155-06-5 trischlorotris(ethyl N-phenyldithiocarbamate)rhodium(III) 
• 91155-13-4 bis(ethyl N-phenyldithiocarbamate)silver(I) nitrate 
• 91155-10-1 bis(ethyl N-phenyldithiocarbamate)bis(triphenylphosphine)platinum⁽⁰⁾ 
• 1152-54-1 N,N-diphenyl-[1,3,4]thiadiazole-2,5-diamine 
• 91155-16-7 dichlorobis(ethyl N-phenyldithiocarbamate)mercury(II) 
• 91155-09-8 bis(ethyl N-phenyldithiocarbamate)bis(triphenylphosphine)palladium⁽⁰⁾ 
• 91155-14-5 dichlorobis(ethyl N-phenyldithiocarbamate)zinc(II) 
• 91155-07-6 monochlorobis(ethyl N-phenyldithiocarbamate)triphenylphosphinerhodium(I) 
• 91161-09-0 dichlorobis(ethyl N-phenyldithiocarbamate) iron(II) 
• 1025476-25-8 (Z)-ethyl 2-oxopropyl phenyldithioimidocarbonate 

Relevant academic research and scientific papers

A comparative study of glycosyl thioimidates as building blocks for chemical glycosylation

Our results indicate that the reactivity and the activation profile of thioimidate glycosyl donors vary significantly depending on the endocyclic heteroatom (N,O,S). Reactivity diminishes in accordance with the following sequence: O > S > N; and this tren

New Heterocyclic Compounds : 5-Oxo/thio-4-aryl-2-phenylimino-1,3,4-dithiazolidines

5-Oxo/thio-4-aryl-2-phenylimino-1,3,4-dithiazolidines (VI and IX) have been prepared by reaction of S-chloro-N-phenylisothiocarbamoyl chloride and triethylamine salts of arylthiocarbamic acids and aryldithiocarbamic acids respectively.VI and IX when boiled with benzylamine give the same product (XI).The structures of all these products have been assigned on the basis of chemical transformations and IR data.Probable mechanisms of these reactions are also suggested.