104496-93-7

Upstream product

• 3004-42-0 5-phenyl-1,3,4-oxadiazole-2(3H)-thione 
• 105-39-5 chloroacetic acid ethyl ester 
• 75-15-0 carbon disulfide 
• 613-94-5 benzoic acid hydrazide 
• 105-36-2 ethyl bromoacetate 
• 3004-42-0 2-Mercapto-5-phenyl-1,3,4-oxadiazole 

Downstream Products

• 1051380-22-3 N-benzoyl-N'-methyl-N'-(4-chlorobenzenesulfonyl)hydrazine 
• 1483-23-4 benzoic acid-(N'-methyl-hydrazide); hydrochloride 
• 102396-51-0 N-benzoyl-N'-methyl-N'-(4-methylbenzenesulfonyl)hydrazine 
• 99361-50-9 2-((5-phenyl-1,3,4-oxadiazole-2-yl)thio)acetic acid 

Relevant academic research and scientific papers

One-pot synthesis of 2-Alkylthio-1,3,4-oxadiazole and Bis-(1,3,4- oxadiazole-2-yl)thio alkyl derivatives from acid hydrazides and CS2

An efficient and one-pot method for synthesis of 2-alkylthio-1,3,4- oxadiazole derivatives in mild conditions is described. Some novel derivatives such as bis-1,3,4-oxadiazole analogs are also synthesized.

5-aryl-1,3,4-oxadiazoline-2(3H)-thiones in reactions with alkyl haloacetates

The reaction of 5-aryl-1,3,4-oxadiazoline-2(3H)-thiones with alkyl haloacetates has been studied. It was shown that the reaction proceeds to give S-substituted products. The effect of the nature of the substituents in the molecules of both the thiones and

A new method of reducing 2-mercapto-substituted 1,3,4-oxadizoles: Synthesis of acylhydrazine derivatives

A new method has been developed for the synthesis of acylhydrazines 5a-g by the reduction of unsymmetrical 1,3,4-oxadiazoles 4a-g by using sodium borohydride/acetic acid combination. Later on, acylhydrazines 5a-g were converted to their corresponding sulfonamide derivatives 6a-d.