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4-(5-Methyl-1,3,4-oxadiazol-2-yl)benzoic acid is a synthetic organic compound characterized by its molecular formula C10H8N2O3. As a derivative of benzoic acid, it features a carboxylic acid group, a benzene ring, and a 1,3,4-oxadiazole ring, which collectively confer a range of chemical properties. These functionalities suggest its potential applicability in diverse fields such as pharmaceuticals, agrochemicals, and materials science. However, comprehensive data on its specific uses, toxicology, and potential hazards are currently limited and may require further research for a thorough understanding.

892502-28-2

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892502-28-2 Usage

Uses

Used in Pharmaceutical Industry:
4-(5-Methyl-1,3,4-oxadiazol-2-yl)benzoic acid is used as a chemical intermediate for the synthesis of various pharmaceutical compounds due to its unique molecular structure and functional groups. Its presence in the molecule can contribute to the development of new drugs with specific therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 4-(5-Methyl-1,3,4-oxadiazol-2-yl)benzoic acid is utilized as a building block for the creation of novel agrochemicals, potentially enhancing crop protection and yield through targeted pest control and other agricultural applications.
Used in Materials Science:
4-(5-Methyl-1,3,4-oxadiazol-2-yl)benzoic acid is employed in materials science for the development of new materials with specific properties. Its chemical structure allows for the engineering of materials with tailored characteristics for use in various applications, such as sensors, coatings, or advanced composites.

Check Digit Verification of cas no

The CAS Registry Mumber 892502-28-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,9,2,5,0 and 2 respectively; the second part has 2 digits, 2 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 892502-28:
(8*8)+(7*9)+(6*2)+(5*5)+(4*0)+(3*2)+(2*2)+(1*8)=182
182 % 10 = 2
So 892502-28-2 is a valid CAS Registry Number.

892502-28-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(5-Methyl-1,3,4-oxadiazol-2-yl)benzoic acid

1.2 Other means of identification

Product number -
Other names 4-(5-methyl-1,3,4-oxadiazol-2-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:892502-28-2 SDS

892502-28-2Relevant articles and documents

Room Temperature Carbonylation of (Hetero) Aryl Pentafluorobenzenesulfonates and Triflates using Palladium-Cobalt Bimetallic Catalyst: Dual Role of Cobalt Carbonyl

Joseph, Jayan T.,Sajith, Ayyiliath M.,Ningegowda, Revanna C.,Shashikanth, Sheena

, p. 419 - 425 (2017/02/10)

An efficient method for the carbonylation of (hetero) aryl pentafluorobenzenesulfonates and triflates under exceptionally mild conditions using palladium/dicobalt octacarbonyl [Pd/Co2(CO)8] has been developed. Besides acting as carbon monoxide (CO) source, Co2(CO)8enhances the reaction rate by accelerating the CO insertion through an in situ generated bimetallic palladium cobalt tetracarbonyl [Pd-Co(CO)4] complex. Under the optimized reaction condition, carbonylation of a wide range of activated and deactivated, as well as sterically hindered and heteroaromatic, substrates proceeded efficiently at room temperature. The high chemoselectivity and improved synthesis of biologically relevant Isoguvacine and Lazabemide intermediates highlights its scope as a valuable synthetic method. The generality of this protocol was further extended to other electrophiles (bromides, chlorides and tosylates). (Figure presented.).

C-3 NOVEL TRITERPENONE WITH C-28 REVERSE AMIDE DERIVATIVES AS HIV INHIBITORS

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Page/Page column 69, (2016/11/21)

Formula (I) The invention relates to C-3 novel triterpenone with C-28 reverse amide derivatives, related compounds, and pharmaceutical compositions useful for the therapeutic treatment of viral diseases and particularly HIV mediated diseases.

NOVEL PIPERAZINE DERIVATIVES AS INHIBITORS OF STEAROYL-CoA DESATURASE

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Page/Page column 78-79, (2009/10/01)

The present invention relates to piperidine derivatives that act as inhibitors of stearoyl-CoA desaturase. The invention also relates to methods of preparing the compounds, compositions containing the compounds, and to methods of treatment using the compounds.

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