2060-64-2 Usage
Uses
Used in Pharmaceutical Industry:
1-Benzothiophene-5-carboxylic acid is used as a key intermediate for the synthesis of various pharmaceuticals, contributing to the development of new drugs due to its unique chemical structure and potential therapeutic properties.
Used in Agrochemical Industry:
In the agrochemical sector, 1-Benzothiophene-5-carboxylic acid is utilized as a precursor in the production of agrochemicals, playing a crucial role in the development of pesticides and other agricultural chemicals to enhance crop protection and yield.
Used in Organic Chemistry Research:
1-Benzothiophene-5-carboxylic acid is employed as a building block in the synthesis of organic compounds, facilitating the exploration of new chemical reactions and the creation of novel organic molecules for various applications in research and industry.
Used in Biological and Pharmacological Studies:
Due to its potential anti-inflammatory and anti-bacterial activities, 1-Benzothiophene-5-carboxylic acid is used in biological and pharmacological research to investigate its effects on various biological systems and its potential use in treating inflammatory and bacterial diseases.
Used in Chemical Production:
1-Benzothiophene-5-carboxylic acid is utilized in the production of a wide range of chemical products across various industries, highlighting its versatility and importance in the chemical manufacturing process.
Check Digit Verification of cas no
The CAS Registry Mumber 2060-64-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,0,6 and 0 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 2060-64:
(6*2)+(5*0)+(4*6)+(3*0)+(2*6)+(1*4)=52
52 % 10 = 2
So 2060-64-2 is a valid CAS Registry Number.
2060-64-2Relevant academic research and scientific papers
Carboxylation of Aromatic and Aliphatic Bromides and Triflates with CO2 by Dual Visible-Light–Nickel Catalysis
Meng, Qing-Yuan,Wang, Shun,K?nig, Burkhard
supporting information, p. 13426 - 13430 (2017/10/07)
We report the efficient carboxylation of bromides and triflates with K2CO3 as the source of CO2 in the presence of an organic photocatalyst in combination with a nickel complex under visible light irradiation at room temperature. The reaction is compatible with a variety of functional groups and has been successfully applied to the synthesis and derivatization of biologically active molecules. In particular, the carboxylation of unactivated cyclic alkyl bromides proceeded well with our protocol, thus extending the scope of this transformation. Spectroscopic and spectroelectrochemical investigations indicated the generation of a Ni0 species as a catalytic reactive intermediate.
