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892502-28-2

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892502-28-2 Usage

General Description

4-(5-Methyl-1,3,4-oxadiazol-2-yl)benzoic acid is a synthetic organic compound with a specific molecular formula of C10H8N2O3. Being a derivative of benzoic acid, it embodies a variety of chemical functionalities including a carboxylic acid group, a benzene ring and a 1,3,4-oxadiazole ring. The presence of these moieties suggests its potential use in various applications such as pharmaceuticals, agrochemicals, and potentially in materials science. However, detailed information regarding its specific usage, toxicology, and hazards is not widely available and might need further investigation.

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.).

NOVEL PIPERAZINE DERIVATIVES AS INHIBITORS OF STEAROYL-CoA DESATURASE

-

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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