21520-97-8

Usage

InChI:InChI=1/C9H8ClN3O2/c10-6-1-3-7(4-2-6)14-5-8-12-13-9(11)15-8/h1-4H,5H2,(H2,11,13)

Upstream product

• 2381-75-1 (4-chlorophenoxy)acetic acid hydrazide 
• 122-88-3 4-Chlorophenoxyacetic acid 
• 563-41-7 semicarbazide hydrochloride 
• 506-68-3 bromocyane 

Downstream Products

• 28004-23-1 2-(4-chloro-phenoxymethyl)-5-oxo-5H-[1,3,4]oxadiazolo[3,2-a]pyrimidine-6-carboxylic acid ethyl ester 
• 87658-04-6 1-[5-(4-Chloro-phenoxymethyl)-[1,3,4]oxadiazol-2-yl]-5-[1-(3-nitro-phenyl)-meth-(Z)-ylidene]-imidazolidine-2,4-dione 
• 87658-02-4 1-[5-(4-Chloro-phenoxymethyl)-[1,3,4]oxadiazol-2-yl]-5-[1-(2-nitro-phenyl)-meth-(Z)-ylidene]-imidazolidine-2,4-dione 
• 87658-01-3 1-[5-(4-Chloro-phenoxymethyl)-[1,3,4]oxadiazol-2-yl]-5-[1-(4-dimethylamino-phenyl)-meth-(Z)-ylidene]-imidazolidine-2,4-dione 
• 87658-00-2 1-[5-(4-Chloro-phenoxymethyl)-[1,3,4]oxadiazol-2-yl]-5-[1-(4-methoxy-phenyl)-meth-(Z)-ylidene]-imidazolidine-2,4-dione 
• 87657-99-6 1-[5-(4-Chloro-phenoxymethyl)-[1,3,4]oxadiazol-2-yl]-5-[1-(4-chloro-phenyl)-meth-(Z)-ylidene]-imidazolidine-2,4-dione 
• 87658-03-5 1-[5-(4-Chloro-phenoxymethyl)-[1,3,4]oxadiazol-2-yl]-5-[1-phenyl-meth-(Z)-ylidene]-imidazolidine-2,4-dione 
• 87657-96-3 1-[5-(4-Chloro-phenoxymethyl)-[1,3,4]oxadiazol-2-yl]-imidazolidine-2,4-dione 
• 87657-92-9 [5-(4-Chloro-phenoxymethyl)-[1,3,4]oxadiazol-2-yl]-urea 
• 28054-08-2 {[5-(4-chloro-phenoxymethyl)-[1,3,4]oxadiazol-2-ylamino]-methylene}-malonic acid diethyl ester 

Relevant academic research and scientific papers

Synthesis and Biological Activity of 2-Substituted 6-Carbethoxy-5(H)-oxo-1,3,4-oxadiazolopyrimidines

Several 2-substituted 6-carbethoxy-5(H)-oxo-1,3,4-oxadiazolopyrimidines (4) have been synthesised by the reaction of 5-substituted 2-amino-1,3,4-oxadiazoles (1) with diethyl ethoxymethylenemalonate (2).These compounds have been screened for their p

Synthesis of new 1-[5-(substituted phenoxymethyl)-1,3,4-oxadiazol-2-yl]-5-(substituted benzylidene)hydantoins as potential anthelminthic agents

Various 1-[5-(substituted phenoxymethyl)-1,3,4-oxadiazol-2-yl]5-(substituted benzylidene)hydantoins have been synthesized. Their activities against Hymenolepis nana infection in rats were tested. Compound 27 was found to be the most active showing 78.0% c