194278-43-8 Usage
Description
3-Benzofurancarboxylic acid, ethyl ester is a colorless to pale yellow liquid chemical compound with the molecular formula C11H10O3, characterized by a faint odor. It is utilized in various industries due to its unique chemical properties and biological activity.
Uses
Used in Food and Beverage Industry:
3-Benzofurancarboxylic acid, ethyl ester is used as a flavoring agent and fragrance ingredient for enhancing the taste and aroma of food and beverages.
Used in Perfume and Cosmetics Industry:
3-Benzofurancarboxylic acid, ethyl ester is used as a key ingredient in the production of perfumes and cosmetics, contributing to their distinct scents and appeal.
Used in Pharmaceutical Industry:
3-Benzofurancarboxylic acid, ethyl ester is used as a raw material for the synthesis of various drugs and pharmaceutical products, playing a crucial role in medicinal chemistry and drug discovery.
Used in Medicinal Chemistry and Drug Discovery:
3-Benzofurancarboxylic acid, ethyl ester is used as a compound with potential applications in medicinal chemistry and drug discovery due to its unique chemical properties and biological activity.
Used in Anti-Inflammatory and Antioxidant Research:
3-Benzofurancarboxylic acid, ethyl ester is studied for its potential anti-inflammatory and antioxidant properties, indicating its possible use in the development of treatments for related conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 194278-43-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,2,7 and 8 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 194278-43:
(8*1)+(7*9)+(6*4)+(5*2)+(4*7)+(3*8)+(2*4)+(1*3)=168
168 % 10 = 8
So 194278-43-8 is a valid CAS Registry Number.
194278-43-8Relevant articles and documents
Rhodium(II)-Catalyzed Reaction of Salicylaldehyde and Its Derivatives with Diazocarbonyl Compounds
Sakhabutdinova,Raskil’dina,Zlotskii,Sultanova
, p. 1772 - 1776 (2018)
Reactions of salicylaldehyde and its cyclic acetals with diazocarbonyl compounds in the presence of copper and rhodium catalysts have been studied. The reaction direction and product yields are determined by the nature of the initial reactants and catalys
