91393-16-7

Basic information

• Product Name: 3-(4-methylphenyl)-1,2,4-Oxadiazole-5-carboxylic acid ethyl ester
• Synonyms: 3-(4-methylphenyl)-1,2,4-Oxadiazole-5-carboxylic acid ethyl ester
• CAS NO: 91393-16-7
• Molecular Weight: 232.239
• Mol File: 91393-16-7.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 3-(4-methylphenyl)-1,2,4-Oxadiazole-5-carboxylic acid ethyl ester(CAS DataBase Reference)
• NIST Chemistry Reference: 3-(4-methylphenyl)-1,2,4-Oxadiazole-5-carboxylic acid ethyl ester(91393-16-7)
• EPA Substance Registry System: 3-(4-methylphenyl)-1,2,4-Oxadiazole-5-carboxylic acid ethyl ester(91393-16-7)

Safety Data

• Hazardous Substances Data: 91393-16-7(Hazardous Substances Data)

Upstream product

• 104-85-8 para-methylbenzonitrile 
• 19227-13-5 (Z)-N'-hydroxy-4-methylbenzimidamide 
• 4755-77-5 Ethyl oxalyl chloride 
• 19227-13-5 p-toluamidoxime 

Downstream Products

• 938000-13-6 3-(p-tolyl)-{1,2,4}oxadiazole-5-carboxylic acid 
• 93332-48-0 (3-p-tolyl-[1,2,4]oxadiazol-5-yl)-carbamic acid benzyl ester 
• 88614-71-5 (3-p-tolyl-[1,2,4]oxadiazol-5-yl)-carbamic acid ethyl ester 
• 90766-02-2 3-p-tolyl-[1,2,4]oxadiazole-5-carbonyl azide 
• 3663-38-5 3-p-tolyl-[1,2,4]oxadiazol-5-ylamine 
• 90916-81-7 3-(4-methylphenyl)-1,2,4-oxadiazole-5-carbohydrazide 

Relevant articles and documents

Design, Synthesis and Antifungal/Nematicidal Activity of Novel 1,2,4-Oxadiazole Derivatives Containing Amide Fragments

Plant diseases that are caused by fungi and nematodes have become increasingly serious in recent years. However, there are few pesticide chemicals that can be used for the joint control of fungi and nematodes on the market. To solve this problem, a series

Ferrocenylethenyl-substituted 1,3,4-oxadiazolyl-1,2,4-oxadiazoles: Synthesis, characterization and DNA-binding assays

This article describes the synthesis, characterization and DNA-binding assays of a series of oxadiazoles derived from (E)-3-ferrocenylacrylic acid. The compounds were obtained in satisfactory yields and characterized by NMR and high resolution mass spectrometry analysis. Additionally, the X-Ray characterization of compound 8a was investigated. A series of ferrocenylethenyl-substituted 1,3,4-oxadiazolyl-1,2,4-oxadiazoles was prepared and studied by UV-visible and electrochemical techniques. The characteristic signals of the redox-active ferrocene/ferrocenium couple were monitored, which allowed verification of the influence of electron-withdrawing oxadiazole heterocycles and their dependence on the 1,2,4-oxadiazole substituent. Also, DNA-binding experiments were performed by UV-vis and emission titrations with ct-DNA.

TRIAZOLE DERIVATIVES HAVING ANTIFUNGAL ACTIVITY, METHOD FOR THE PREPARATION THEREOF, AND PHARMACEUTICAL COMPOSITION COMPRISING THE SAME

A triazole derivative of formula 1 or a pharmaceutically acceptable salt, hydrate, solvate or isomer thereof is superior to the conventional antifungal drugs in antifungal activity against a wide spectrum of pathogenic fungi, and has advantageously low toxicity.