904541-27-1

Upstream product

• 21398-09-4 2-(3',4',5'-trimethoxyphenyl)-5-(p-nitrophenyl)-1,3,4-oxadiazole 
• 122-04-3 4-nitro-benzoyl chloride 
• 3291-03-0 3,4,5-trimethoxybenzohydrazide 
• 86-81-7 3,4,5-trimethoxy-benzaldehyde 
• 5351-17-7 4-aminobenzohydrazide 
• 150-13-0 4-amino-benzoic acid 
• 94-09-7 p-aminoethylbenzoate 
• 220307-56-2 4-Nitro-benzoic acid [1-(3,4,5-trimethoxy-phenyl)-meth-(E)-ylidene]-hydrazide 
• 356526-82-4 3,4,5-trimethoxy-N'-(4-nitrobenzoyl)benzohydrazide 

Downstream Products

• 1333868-35-1 4-(2-(4-(5-(3,4,5-trimethoxyphenyl)-1,3,4-oxadiazol-2-yl)phenylamino)ethoxy)-2H-chromen-2-one 

Relevant academic research and scientific papers

Light-controlled fungicide for controlling plant fungal diseases and application thereof

The invention belongs to the field of light-controlled pesticide fungicides, and discloses a light-controlled fungicide for controlling plant fungal diseases and application thereof. The fungicide has a structure as shown in the chemical formula I, and is

Light-control plant disease prevention and control sterilization agent with 1,3,4-oxadiazole azobenzene and application

The invention belongs to the field of light-control pesticide sterilization agents and discloses a light-control plant disease prevention and control sterilization agent with 1,3,4-oxadiazole azobenzene and application. The sterilization agent is of a str

Synthesis and biological evaluation of 1,3,4-oxadiazole derivatives as novel analgesic and antiinflammatory agents

A novel series of 4-(2-(4-(5-(4-substituted phenyl)-1,3,4-oxadiazol-2-yl) phenylamino)ethoxy)-2H-chromen-2-one (7a-j) have been synthesized from 4-(5-(4-substituted phenyl)-1,3,4-oxadiazol-2-yl)benzenamine (4a-j) and 4-(2-bromoethoxy)-2H-chromen-2-one (5). The synthesized compounds were characterized on the basis of their spectral (IR, 1H NMR) data and evaluated for the anti-inflammatory and analgesic activity by using different pharmacological models. The most active compounds were subjected to acute ulcerogenesis activity and were found to be less ulcerogenic than the standard.

Synthesis, anti-HIV, and antifungal activity of new benzensulfonamides bearing the 2,5-disubstituted-1,3,4-oxadiazole moiety

A series of novel chiral and achiral N-[1-(1,3,4-oxadiazol-2ylthio)alkyl]- 4-methyl/chloro/methoxybenzenesulfonamides 5a-l were prepared by the reaction of 4-(4-methyl, chloro, methoxyphenylsulfonamido)alkyl carboxylic acid hydrazides 4a-l with CS2 and KO