24028-40-8

Usage

InChI:InChI=1/C8H6N2OS/c11-8-10-9-7(12-8)6-4-2-1-3-5-6/h1-5H,(H,10,11)

Upstream product

• 86738-35-4 2-(methylsulfonyl)-5-phenyl-1,3,4-thiadiazole 
• 64145-06-8 (5-phenyl-1,3,4-thiadiazol-2-yl-sulfanyl)acetic acid 
• 109142-08-7 1-thiobenzoyl semicarbazide 
• 64145-14-8 (phenyl-[1,3,4]thiadiazole-2-sulfonyl)-acetic acid ethyl ester 
• 10465-97-1 N-benzoyl-N'-ethoxycarbonyl hydrazine 
• 49580-00-9 2-benzylidene-1-(5-phenyl-1,3,4-thiadiazol-2-yl)hydrazine 
• 97051-23-5 2-ethylsulfonyl-5-phenyl-1,3,4-thiadiazole 
• 1925-69-5 2-Methoxy-5-phenyl-1,3,4-thiadiazol 
• 5333-86-8 ethyl benzimidate hydrochloride 
• 98-88-4 benzoyl chloride 
• 2002-03-1 2-amino-5-phenyl-1,3,4-thiadiazole 
• 1627-73-2 1-benzylidene thiosemicarbazide 
• 13373-11-0 2-chloro-5-phenyl-[1,3,4]thiadiazole 
• 13097-06-8 N-(4-oxo-2-sulfanylidene-1,3-thiazolidin-3-yl)benzamide 

Downstream Products

• 82476-09-3 2-phenyl-4-ethyl-1,3,4-thiadiazol-5(4H)-one 
• 53645-95-7 2-bromo-5-phenyl-1,3,4-thiadiazole 
• 134785-99-2 2-phenyl-4-ethoxycarbonyl-1,3,4-thiadiazol-5(4H)-one 
• 97051-27-9 2-phenyl-4-propargyl-1,3,4-thiadiazolin-5-one 
• 120590-05-8 2-<2-oxo-5-phenyl-1,3,4-thiadiazol-3(2H)-yl>propionic acid ethyl ester 
• 99361-51-0 (phenyl-[1,3,4]thiadiazol-2-yloxy)-acetic acid 
• 97051-05-3 5-Phenyl-3-(4-pyrrolidin-1-yl-but-2-ynyl)-3H-[1,3,4]thiadiazol-2-one 
• 97051-06-4 5-Phenyl-3-(4-piperidin-1-yl-but-2-ynyl)-3H-[1,3,4]thiadiazol-2-one 
• 97051-11-1 3-(4-Morpholin-4-yl-but-2-ynyl)-5-phenyl-3H-[1,3,4]thiadiazol-2-one 
• 97051-07-5 3-[4-(2-Methyl-piperidin-1-yl)-but-2-ynyl]-5-phenyl-3H-[1,3,4]thiadiazol-2-one; hydrochloride 
• 97051-09-7 3-(4-Azepan-1-yl-but-2-ynyl)-5-phenyl-3H-[1,3,4]thiadiazol-2-one; hydrochloride 
• 97051-08-6 3-[4-((2S,6R)-2,6-Dimethyl-piperidin-1-yl)-but-2-ynyl]-5-phenyl-3H-[1,3,4]thiadiazol-2-one; hydrochloride 
• 97051-10-0 3-[4-(4-Methyl-piperazin-1-yl)-but-2-ynyl]-5-phenyl-3H-[1,3,4]thiadiazol-2-one; hydrochloride 
• 96134-33-7 N,N-diethyl-5-phenyl-1,3,4-thiadiazol-2-amine 

Relevant academic research and scientific papers

Halopropargyl compounds, compositions, uses and processes of preparation

Compounds of the formula STR1 wherein A is selected from the group consisting of hydrogen, alkyl, aryl, and heterocyclic; Y and Z are independently selected from the group consisting of O, S, and N--R; R is selected from the group consisting of hydrogen,

The Oxidation of 1-Thioaroylsemicarbazides

Oxidation of 1-thioaroylsemicarbazides by bromine or hydrogen peroxide yields bis(C-aryl-N-ureido)formimidoyl disulphides.As a novel class of the generally labile di-imidoyl disulphides, such products display unusual stability; however, upon acylation, me

Synthesis and biological evaluation of 5-aryl-3-(4-tert-amino-2-butynyl)-1,3,4-thiadiazol-2 (3H)-ones

A series of 5-aryl-3-(4-tert-amino-2-butynyl)-1,3,4-thiadiazol-2 (3H)-ones has been prepared and investigated for blocking motor effects of oxotremorine in intact mice and for their antagonistic activity towards acetylcholine on isolated guinea pig ileal

Studies on organophosphorus compounds XLIX. An improved method for the preparation of 2,5-disubstituted 1,3,4-thiadiazoles and 1,3,4-thiadiazole-2(3H)-thiones

The reaction of 2,4-bis(4-methoxyphenyl)-1,3,2,4-dithiadiphosphetane 2,4-disulfide (LR) with N,N'-diacylhydrazines and N-acyl-N'-ethoxycarbonyl hydrazines has been investigated.It is shown that 2,5-disubstituted-1,3,4-thiadiazoles and 5-phenyl-1,3,4-thiadiazole-2(3H)-thione are produced in good yields.However, in the case of N-acetyl-N'-ethoxycarbonylhydrazine a 2,3-dihydro-1,3,4,2-thiadiazaphosphole, X, is formed.The fragmentation patterns in the mass spectra of simple 2,5-disubstituted 1,3,4,-thiadiazoles, IIIa-f, are described.

Unsaturated Compounds containing Nitrogen. Part 4. Further Reactions of 1-Chloro-2,3-diazabutadienes with S-Nucleophiles

1-Chloro-1,4-diaryl-2,3-diazabutadienes (Ar1CCl=NN=CHAr2), prepared by the reaction of thionyl chloride with aroylhydrazones (Ar1CONHN=CHAr2), react with thiosemicarbazide or thiocarbohydrazide to give 2-arylidenehydrazino-5-aryl-1,3,4-thiadiazoles, and with potassium thiocyanate to give 1-thiocyanato-1,4-diaryl-2,3-diazabutadienes which isomerize thermally to arylideneamino-5-aryl-1,3,4-thiadiazoles. 1-Chloro-1,4-diphenyl-2,3-diazabutadiene reacts with potassium ethylxanthate to give a 1-ethylxanthyl-2,3-diazabutadiene which on pyrolysis yields 2,5-diphenyl-1,3,4-thiadiazole.