4955-82-2

Usage

InChI:InChI=1/C8H6N2S/c9-6-8(11)10-7-4-2-1-3-5-7/h1-5H,(H,10,11)

Upstream product

• 151-50-8 potassium cyanide 
• 103-72-0 phenyl isothiocyanate 
• 10543-64-3 phenyl-oxalamide 
• 1457-46-1 3-phenylrhodanine 
• 125244-74-8 oxanilic acid thioamide 
• 17270-94-9 N-Phenyldithiooxamide 
• 64-17-5 ethanol 

Downstream Products

• 65101-10-2 N-benzoyl-N-phenylcyanothioformamide 
• 6343-76-6 1-cyano-N,N-diphenylformamidine 
• 4955-83-3 methyl-phenyl-thiooxalamonitrile 
• 17270-94-9 N-Phenyldithiooxamide 
• 10543-64-3 phenyl-oxalamide 
• 90345-46-3 2-(phenylamino)-2-thiooxoacetamide 
• 61522-23-4 2-cyano-4-oxo-3,5-diphenyl-4,5-dihydro-thiazolium betaine 
• 25309-98-2 Benzyl--disulfid 
• 6784-22-1 phenylcarbamoyl cyanide 
• 76968-20-2 5-Imino-2,3-diphenyl-oxazolidine-4-thione 
• 74331-41-2 5-Imino-1,3-diphenyl-2,4-imidazolidinedithione 
• 87606-14-2 3-phenyl-4-imino-5-(phenylimino)-2-thiazolidinethione 
• 116708-95-3 3-(3,4-dichlorophenyl)-4-imino-5-(phenylimino)-2-thiazolidinethione 
• 97012-44-7 3-methyl-4-imino-5-(phenylimino)-2-thiazolidinethione 

Relevant academic research and scientific papers

New imidazolidineiminothione derivatives: Synthesis, spectral characterization and evaluation of antitumor, antiviral, antibacterial and antifungal activities

A series of new imidazolidineiminothione derivatives with various halogenated and alkylated aromatic substituents at N-(1) and at N-(3) was synthesized through the reaction of N-arylcyanothioformamides with arylisocyanate derivatives. Structure of imidazo

Studies on 4-thiazolidinones: Scope of the reactions of 3-aryl-2-thioxo-1,3-thiazolidin-4-ones with cyanide and cyanate ions

Treatment of 3-aryl-2-thioxo-1,3-thiazolidin-4-ones 1 with CN- and NCO- effected the ring cleavage providing [(cyanocarbonothioyl) amino]benzenes 4 and arylisothiocyanates 5, respectively. Similar treatment of 5-(2-aryl-2-oxoethyl) derivatives 2 afforded 2,4-bis(2-aryl-2-oxoethylidene) cyclobutane-1,3-diones 6 along with each of the preceding products. Treatment of the respective (E,Z)-5-(2-aryl-2-oxoethylidene) analogues 3b and 3c with CN- gave 4b and 4c and 2-(arylcarbonyl)-2-methoxy-4- oxopentanedinitriles 7b and 7c, in addition to 3,6-bis[2-(4-chlorophenyl)-1- methoxy-2-oxoethylidene]-1,4-dithiane-2,5-dione 8c, which has been generated from 3c. Reactions of 3c or 3d with NCO- provided 5c or 5d, together with 8c or 8d as pure isomers. In the formation of the MeO products 7 and 8, the solvent (MeOH) has participated. Structures of these products are based on microanalytical and spectroscopic data. Rationalizations for the above transformations are given.

Certain 4-halo-5-aryl-1,2,3-dithiazole compounds and their preparation

4-HALO-5-ARYL-1,2,3-DITHIAZOLE, USEFUL AS FUNGICIDES, OVICIDES, INSECTICIDES AND HERBICIDES, ARE PREPARED BY REACTING A N-aryl cyanothioformamide and a sulfur dihalide in the presence of a catalytic amount of a formamide compound or quaternary ammonium sa