861146-16-9

Basic information

• Product Name: 3-(4-fluorophenyl)-1,2,4-oxadiazole-5-carbohydrazide
• Synonyms: 3-(4-fluorophenyl)-1,2,4-oxadiazole-5-carbohydrazide
• CAS NO: 861146-16-9
• Molecular Weight: 222.179
• Mol File: 861146-16-9.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 3-(4-fluorophenyl)-1,2,4-oxadiazole-5-carbohydrazide(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-fluorophenyl)-1,2,4-oxadiazole-5-carbohydrazide(861146-16-9)
• EPA Substance Registry System: 3-(4-fluorophenyl)-1,2,4-oxadiazole-5-carbohydrazide(861146-16-9)

Safety Data

• Hazardous Substances Data: 861146-16-9(Hazardous Substances Data)

Upstream product

• 1194-02-1 4-fluorobenzonitrile 
• 22179-78-8 4-fluoro-benzamidoxime 
• 861146-13-6 3-(4-fluoro-phenyl)-[1,2,4]oxadiazole-5-carboxylic acid methyl ester 

Downstream Products

• 1187736-34-0 5-[3-(4-fluorophenyl)-1,2,4-oxadiazol-5-yl]-2-(N-phenylamino)-1,3,4-oxadiazole 
• 1187736-26-0 N₁-[3-(4-fluorophenyl)-1,2,4-oxadiazol-5-ylcarbonyl]-N₄-phenyl thiosemicarbazide 

Relevant articles and documents

Conjugation of N-acylhydrazone and 1,2,4-oxadiazole leads to the identification of active antimalarial agents

Malaria, caused by several Plasmodium species, is the major life-threatening parasitic infection worldwide. Due to the parasite resistance to quinoline based drugs, the search for antimalarial agents is necessary. Here, we report the structural design, sy

NOVEL NK-3 RECEPTOR SELECTIVE ANTAGONIST COMPOUNDS, PHARMACEUTICAL COMPOSITION AND METHODS FOR USE IN NK-3 RECEPTORS MEDIATED DISORDERS

The present invention is directed to novel compounds of formula I and their use as therapeutic compounds.

Synthesis, biological evaluation, and structural studies of 3-phenyl[1,2,4]oxadiazole-5-carboxylic acid benzo[1,3]dioxol 5-ylmethylene-hydrazide

A series of 1,2,4-oxadiazole combined with carbohydrazides residues, designed as possible bioactive compounds, was obtained in an attempt to analyse the effects of this molecular hybridization on the biological properties of the resulting compounds. They