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Benzoic acid, 4-(5-ethyl-1,2,4-oxadiazol-3-yl)(9CI) is a chemical compound with the molecular formula C10H10N2O3. It is a derivative of benzoic acid, which is known for its use as a food preservative and for its antimicrobial properties. The 4-(5-ethyl-1,2,4-oxadiazol-3-yl) group in Benzoic acid, 4-(5-ethyl-1,2,4-oxadiazol-3-yl)- (9CI) is a heterocyclic ring that may have potential pharmaceutical applications. This chemical compound is characterized by its unique structure and properties, which could be explored for various applications in different industries.

769132-76-5

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769132-76-5 Usage

Uses

Used in Pharmaceutical Industry:
Benzoic acid, 4-(5-ethyl-1,2,4-oxadiazol-3-yl)(9CI) is used as a potential pharmaceutical compound for its potential medicinal properties. The heterocyclic ring in Benzoic acid, 4-(5-ethyl-1,2,4-oxadiazol-3-yl)- (9CI) may offer unique therapeutic benefits, and further research and testing would be needed to determine its specific applications and benefits in the pharmaceutical field.
Used in Food Preservation:
Benzoic acid, 4-(5-ethyl-1,2,4-oxadiazol-3-yl)(9CI) is used as a food preservative due to its antimicrobial properties. Benzoic acid, 4-(5-ethyl-1,2,4-oxadiazol-3-yl)(9CI) can help extend the shelf life of food products by inhibiting the growth of bacteria, yeast, and molds, ensuring the safety and quality of the food.
Used in Antimicrobial Applications:
In addition to its use in food preservation, Benzoic acid, 4-(5-ethyl-1,2,4-oxadiazol-3-yl)(9CI) can also be used in various antimicrobial applications. Benzoic acid, 4-(5-ethyl-1,2,4-oxadiazol-3-yl)(9CI)'s ability to inhibit the growth of microorganisms makes it suitable for use in medical, industrial, and environmental settings to prevent the spread of infections and maintain cleanliness.
Used in Chemical Synthesis:
Benzoic acid, 4-(5-ethyl-1,2,4-oxadiazol-3-yl)(9CI) can be used as a starting material or intermediate in the synthesis of other chemical compounds. Its unique structure and properties may be utilized in the development of new pharmaceuticals, agrochemicals, or other specialty chemicals, contributing to the advancement of various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 769132-76-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,6,9,1,3 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 769132-76:
(8*7)+(7*6)+(6*9)+(5*1)+(4*3)+(3*2)+(2*7)+(1*6)=195
195 % 10 = 5
So 769132-76-5 is a valid CAS Registry Number.
InChI:InChI=1/C11H10N2O3/c1-2-9-12-10(13-16-9)7-3-5-8(6-4-7)11(14)15/h3-6H,2H2,1H3,(H,14,15)

769132-76-5 Well-known Company Product Price

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  • Alfa Aesar

  • (H50744)  4-(5-Ethyl-1,2,4-oxadiazol-3-yl)benzoic acid, 97%   

  • 769132-76-5

  • 250mg

  • 515.0CNY

  • Detail
  • Alfa Aesar

  • (H50744)  4-(5-Ethyl-1,2,4-oxadiazol-3-yl)benzoic acid, 97%   

  • 769132-76-5

  • 1g

  • 2057.0CNY

  • Detail

769132-76-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-(5-Ethyl-1,2,4-Oxadiazol-3-yl)Benzoic Acid

1.2 Other means of identification

Product number -
Other names 4-(5-Ethyl-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:769132-76-5 SDS

769132-76-5Downstream Products

769132-76-5Relevant articles and documents

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.

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