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89546-87-2

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89546-87-2 Usage

Description

3-(5-Methyl-[1,3,4]oxadiazol-2-yl)-pyridine is a heterocyclic chemical compound with the molecular formula C8H7N3O. It is a pyridine derivative featuring a substituted oxadiazole ring, which contributes to its unique structure and properties. 3-(5-Methyl-[1,3,4]oxadiazol-2-yl)-pyridine is composed of carbon, hydrogen, nitrogen, and oxygen atoms, and it has potential applications in various fields, including pharmacology and drug development, due to its ability to interact with biological systems. Its reactivity and functional groups also suggest possible uses in other industries, such as agriculture and materials science.

Uses

Used in Pharmaceutical Industry:
3-(5-Methyl-[1,3,4]oxadiazol-2-yl)-pyridine is used as a building block for the synthesis of new pharmaceutical compounds. Its unique structure and properties make it valuable in the development of novel drugs that can interact with biological systems, potentially leading to the creation of new treatments for various diseases and conditions.
Used in Drug Development:
3-(5-Methyl-[1,3,4]oxadiazol-2-yl)-pyridine is used as a component in drug development for its potential to contribute to the creation of innovative medications. Its ability to interact with biological systems makes it a promising candidate for the design of new drugs that can target specific pathways or receptors in the body.
Used in Research and Development:
3-(5-Methyl-[1,3,4]oxadiazol-2-yl)-pyridine is used as a subject of research and development in various fields, including medicine, agriculture, and materials science. Its reactivity and functional groups make it a versatile compound for exploring new applications and understanding its potential impact on different industries.
Used in Industrial Applications:
3-(5-Methyl-[1,3,4]oxadiazol-2-yl)-pyridine is used in industrial applications due to its reactivity and functional groups. Its potential uses in this area may include the development of new materials, catalysts, or other products that can benefit from its unique chemical properties. Further research and development are necessary to fully explore and understand the compound's capabilities in these applications.

Check Digit Verification of cas no

The CAS Registry Mumber 89546-87-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,5,4 and 6 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 89546-87:
(7*8)+(6*9)+(5*5)+(4*4)+(3*6)+(2*8)+(1*7)=192
192 % 10 = 2
So 89546-87-2 is a valid CAS Registry Number.

89546-87-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-methyl-5-pyridin-3-yl-1,3,4-oxadiazole

1.2 Other means of identification

Product number -
Other names -

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:89546-87-2 SDS

89546-87-2Relevant articles and documents

TiCl4 mediated facile synthesis of 1,3,4-oxadiazoles and 1,3,4-thiadiazoles

Zhang, Lin,Yu, Yu,Tang, Qiang,Yuan, Jianyong,Ran, Dongzhi,Tian, Binghua,Pan, Tao,Gan, Zongjie

, p. 423 - 431 (2019/12/27)

An efficient method for the synthesis of 2,5-disubstituted 1,3,4-oxadiazoles and 1,3,4-thiadiazoles has been developed. Various hydrazides or thionyl hydrazides readily react with DMA derivatives in the presence of TiCl4 as a catalyst to afford the desired products. This protocol provides a simple and economical procedure that affords the target products with good yields and wide substrate scope.

Trifluoromethanesulfonic acid-Ag(I) complex based on 3-(5-methyl-1,3,4-oxadiazole)pyridine and synthetic method thereof

-

Paragraph 0023; 0024; 0025, (2018/03/01)

The invention discloses a trifluoromethanesulfonic acid-Ag(I) complex based on 3-(5-methyl-1,3,4-oxadiazole)pyridine and a synthetic method thereof. The trifluoromethanesulfonic acid-Ag(I) complex hasa general chemical formula of {[Ag3(L)4].3CF3SO3}, wherein L is 3-(5-methyl-1,3,4-oxadiazole)pyridine used as a ligand. The synthetic method comprises the following steps: weighing AgCF3SO3 and the ligand namely 3-(5-methyl-1,3,4-oxadiazole)pyridine according to a mol ratio as shown in the general chemical formula of {[Ag3(L)4].3CF3SO3}, carrying out uniform mixing, carrying out a reaction at 150to 180 DEG C, and carrying out natural cooling to a room temperature of 20 to 25 DEG C so as to obtain a white transparent crystal, i.e., the complex provided by the invention. The complex provided by the invention shows adsorption properties to a variety of dyes, and has application potential.

Syntheses, structural diversities and characterization of a series of coordination polymers with two isomeric oxadiazol-pyridine ligands

Ding, Bin,Wu, Jie,Wu, Xiang Xia,Huo, Jian Zhong,Zhu, Zhao Zhou,Liu, Yuan Yuan,Shi, Fang Xue

, p. 9704 - 9718 (2017/02/15)

In this work two positional-isomeric oxadiazol-pyridine ligands 3-(5-methyl-1,3,4-oxadiazol-2-yl)pyridine (L1) and 4-(5-methyl-1,3,4-oxadiazol-2-yl)pyridine (L2) have been designed and synthesized. A series of novel coordination polymers, namely [Cd2(μ2-L1)2(μ2-NCS)4]n (1), {[Cd(L1)(μ2-dca)2(H2O)]·H2O}n (2), {[Cu(μ2-L1)2(NCS)2]·0.5H2O}n (3), {[Ag2(μ2-L1)(μ3-L1)2]·2PF6}n (4), {[Ag3(μ2-L1)4(μ2-CF3SO3)(CF3SO3)]·CF3SO3} (5), {[Cd(L2)2(μ2-NCS)2]}n (6), [Ag(μ2-L2)(μ2-CF3SO3)]n (7) and {[Ag(μ2-L2)]·BF4}n (8) have been isolated. Both 1 and 2 are 2D CdII coordination polymers containing infinite {Cd-NCS-Cd} chains (for 1) or infinite {Cd-dca-Cd} layers (for 2), respectively. 3 is a 2D CuII coordination polymer, in which central metal ions are bridged via a bidentate bridging L1 ligand. While when different AgI salts were introduced into the reaction system, 1D AgI coordination polymers 4 and 5 with diverse coordination modes can be isolated. Furthermore, when the isomeric oxadiazol-pyridine L2 is used to replace L1 in the reaction system, 6-8 can be isolated. 6 is a 2D CdII coordination polymer containing {Cd-NCS-Cd} layers. 7 is a 2D neutral AgI coordination polymer while 8 is a 2D cationic AgI coordination polymer. Variable temperature magnetic susceptibility measurements (2-300 K) reveal anti-ferromagnetic interactions between central copper(ii) ions for 3. Solid-state luminescent properties of 1, 2 and 4-8 have been investigated indicating strong fluorescent emissions. Additionally, luminescent measurements illustrate that complex 8 exhibits highly sensitive luminescence sensing for Cr2O72? ions in aqueous solutions with high quenching efficiency Ksv = 2.08 × 104 L mol?1 and low detection limit (0.19 μM (S/N = 3)). 8 also represents the first report of a coordination polymer based on oxadiazol-pyridine derivatives with a luminescence response to Cr2O72? anion pollutants in aqueous solutions.

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