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3-(5-Methyl-1,2,4-oxadiazol-3-yl)benzoic acid is a chemical compound belonging to the oxadiazole class, which are heterocyclic compounds containing non-carbon atoms within a carbon-containing molecule. As a benzene derivative, 3-(5-METHYL-1,2,4-OXADIAZOL-3-YL)BENZOIC ACID features a carboxyl group (-COOH), exhibiting moderate acidity. Its molecular and physical properties can be influenced by the nature of substituents, and its chemical properties and applications may vary widely depending on its structure and reactions with other chemicals.

264264-32-6

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264264-32-6 Usage

Uses

Used in Chemical Synthesis:
3-(5-Methyl-1,2,4-oxadiazol-3-yl)benzoic acid is used as a building block in the synthesis of various organic compounds, including pharmaceuticals, agrochemicals, and other specialty chemicals. Its unique structure and reactivity make it a valuable intermediate in the development of new molecules with specific properties and applications.
Used in Pharmaceutical Industry:
In the pharmaceutical industry, 3-(5-Methyl-1,2,4-oxadiazol-3-yl)benzoic acid is used as a key component in the development of new drugs. Its oxadiazole and benzoic acid moieties can be exploited to design molecules with potential therapeutic effects, such as anti-inflammatory, antimicrobial, or anticancer properties. 3-(5-METHYL-1,2,4-OXADIAZOL-3-YL)BENZOIC ACID's moderate acidity and reactivity with other functional groups can be utilized to optimize the drug's pharmacokinetic and pharmacodynamic properties.
Used in Material Science:
3-(5-Methyl-1,2,4-oxadiazol-3-yl)benzoic acid can be used in material science for the development of novel materials with specific properties. Its unique structure and reactivity can be employed to create polymers, coatings, or other materials with tailored characteristics, such as thermal stability, chemical resistance, or specific optical or electronic properties.
Used in Analytical Chemistry:
In analytical chemistry, 3-(5-Methyl-1,2,4-oxadiazol-3-yl)benzoic acid can be used as a reagent or a reference compound in various analytical techniques. Its unique chemical properties, such as its moderate acidity and reactivity, can be exploited for the development of new methods for the detection, quantification, or separation of different compounds.
Used in Research and Development:
3-(5-Methyl-1,2,4-oxadiazol-3-yl)benzoic acid is used as a research compound in various scientific studies, exploring its potential applications and properties. Researchers can investigate its reactivity, stability, and interactions with other chemicals, as well as its potential use in the development of new materials, drugs, or other products.

Check Digit Verification of cas no

The CAS Registry Mumber 264264-32-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,6,4,2,6 and 4 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 264264-32:
(8*2)+(7*6)+(6*4)+(5*2)+(4*6)+(3*4)+(2*3)+(1*2)=136
136 % 10 = 6
So 264264-32-6 is a valid CAS Registry Number.
InChI:InChI=1/C10H8N2O3/c1-6-11-9(12-15-6)7-3-2-4-8(5-7)10(13)14/h2-5H,1H3,(H,13,14)

264264-32-6 Well-known Company Product Price

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  • Alfa Aesar

  • (H50832)  3-(5-Methyl-1,2,4-oxadiazol-3-yl)benzoic acid, 98%   

  • 264264-32-6

  • 250mg

  • 571.0CNY

  • Detail
  • Alfa Aesar

  • (H50832)  3-(5-Methyl-1,2,4-oxadiazol-3-yl)benzoic acid, 98%   

  • 264264-32-6

  • 1g

  • 2286.0CNY

  • Detail

264264-32-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 3-(5-METHYL-1,2,4-OXADIAZOL-3-YL)BENZOIC ACID

1.2 Other means of identification

Product number -
Other names 3-(5-Methyl-1,2,4-oxadiazol-3-yl)benzoic acid

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:264264-32-6 SDS

264264-32-6Relevant academic research and scientific papers

Synthesis of benzoic acids containing a 1,2,4-oxadiazole ring

Krasouskaya,Danilova,Baikov,Kolobov,Kofanov

, p. 142 - 145 (2015/10/05)

A new approach to the synthesis of 4and 3-(5-R-1,2,4-oxadiazol-3-yl)benzoic acids via a selective oxidation of 5-R-3-tolyl-1,2,4-oxadiazoles with air oxygen in the presence of a catalytic system based on cobalt acetate was suggested. This synthesis allowed us to obtain the products in higher yields and with shorter sequence of steps as compared to the known procedures.

BENZOTHIAZOLONE DERIVATIVES

-

Page/Page column 19, (2011/11/12)

Compounds of the formula I, in which R1, R2, R3, R3′, R4, R4′, E, E′, E″ and E′″ have the meanings indicated in Claim 1, are inhibitors of tyrosine kinases, in particular Met kinase, and ca

Pyridazinone derivatives

-

, (2011/11/12)

Compounds of the formula (I) in which D, R1, R2, R3, R4 have the meanings indicated in Claim 1, are inhibitors of tyrosine kinases, in particular of Met kinase, and can be employed, inter alia, for the treatment

2-BENZYLPYRIDAZINONE DERIVATIVES AS MET KINASE INHIBITORS

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Page/Page column 24, (2010/12/26)

Compounds of the formula I in which R1, R2, R3, R4′ have the meanings indicated in claim 1, are inhibitors of tyrosine kinases, in particular Met kinase, and can be employed, inter alia, for the treatment of tumours.

2-OXO-3-BENZYLBENZOXAZOL-2-ONE DERIVATIVES AND RELATED COMPOUNDS AS MET KINASE INHIBITORS FOR THE TREATMENT OF TUMOURS

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Page/Page column 40, (2010/12/29)

Compounds of the formula (I), in which R1, R2, R3, R3′, R4, R4′, E, E′, E″ and E′″ have the meanings indicated in Claim 1, are inhibitors of tyrosine kinases, in particular Met kinase, and can be employed, inter alia, for the treatment of tumours.

M3 MUSCARINIC ACETYLCHOLINE RECEPTOR ANTAGONISTS

-

Page/Page column 26-27, (2010/02/14)

Muscarinic Acetylcholine receptor antagonists and methods of using them are provided.

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