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5-Pyridin-3-yl-1,2,4-oxadiazol-3-amine is a heterocyclic chemical compound with the molecular formula C7H6N4O. It features a pyridine ring fused to an oxadiazole ring, which contributes to its unique chemical and biological properties. 5-Pyridin-3-yl-1,2,4-oxadiazol-3-amine is of significant interest in medicinal chemistry due to its potential for exhibiting various biological activities, making it a promising candidate for the development of pharmaceuticals and agrochemicals.

73631-18-2

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73631-18-2 Usage

Uses

Used in Pharmaceutical and Agrochemical Synthesis:
5-Pyridin-3-yl-1,2,4-oxadiazol-3-amine is used as a building block in the synthesis of pharmaceuticals and agrochemicals for its potential to contribute to the development of new drugs and pesticides. Its unique structure allows for the creation of diverse molecules with potential therapeutic or pesticidal properties.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 5-Pyridin-3-yl-1,2,4-oxadiazol-3-amine is used as a research target to explore its potential biological activities. Its specific properties make it valuable for investigating new mechanisms of action and for the discovery of novel therapeutic agents.
Used as a Fluorescent Probe:
5-Pyridin-3-yl-1,2,4-oxadiazol-3-amine has been studied for its potential applications as a fluorescent probe. Its fluorescent properties can be utilized in various analytical techniques, such as fluorescence spectroscopy and imaging, to detect and monitor biological processes or to study the interactions of molecules with biological targets.
Used in Material Science:
5-Pyridin-3-yl-1,2,4-oxadiazol-3-amine is also of interest in material science for its potential use in the development of new materials. Its unique structure and properties may contribute to the creation of advanced materials with specific characteristics, such as high thermal stability, optical properties, or other desirable traits for various applications.

Check Digit Verification of cas no

The CAS Registry Mumber 73631-18-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,6,3 and 1 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 73631-18:
(7*7)+(6*3)+(5*6)+(4*3)+(3*1)+(2*1)+(1*8)=122
122 % 10 = 2
So 73631-18-2 is a valid CAS Registry Number.
InChI:InChI=1/C7H6N4O/c8-7-10-6(12-11-7)5-2-1-3-9-4-5/h1-4H,(H2,8,11)

73631-18-2SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-pyridin-3-yl-1,2,4-oxadiazol-3-amine

1.2 Other means of identification

Product number -
Other names 5-(pyridin-3-yl)-1,2,4-oxadiazol-3-amine

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:73631-18-2 SDS

73631-18-2Downstream Products

73631-18-2Relevant academic research and scientific papers

Facile synthesis of 3-amino-5-aryl-1,2,4-oxadiazoles: Via PIDA-mediated intramolecular oxidative cyclization

Lu, Kuan,Duan, Liancheng,Xu, Boxuan,Yin, Weile,Wu, Di,Zhao, Yanfang,Gong, Ping

, p. 54277 - 54280 (2016/07/06)

A mild and efficient method for the synthesis of 3-amino-5-aryl-1,2,4-oxadiazole by intramolecular cyclization using PhI(OAc)2 (PIDA) as an oxidant is developed. Various 3-amino-5-aryl-1,2,4-oxadiazoles are prepared in moderate to good yields,

Synthesis and Diuretic Profile of 3-(3-Amino-1,2,4-oxadiazol-5-yl)-5-chloro-2,6-pyrazinediamine, an Amiloride-Type Diuretic

Watthey, Jeffrey W. H.,Desai, Mahesh,Rutledge, Richard,Dotson, Ronald

, p. 690 - 692 (2007/10/02)

The synthesis of an analogue of amiloride in which the acylguanidine moiety has been replaced by a 1,2,4-oxadiazol-3-amine unit is described.This substance (3, CGS 4270) exhibited a diuretic profile similar to that of amiloride when evaluated in the rat a

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