306955-85-1 Usage
Uses
Used in Pharmaceutical Research and Drug Development:
2-(3-(TrifluoroMethyl)phenylsulfonaMido)benzoic acid is used as a research compound for its potential pharmacological properties. It has been studied for its anti-inflammatory and analgesic effects, making it a candidate for the development of drugs to treat conditions such as arthritis and chronic pain.
Used in the Synthesis of New Pharmaceutical Compounds and Bioactive Molecules:
Due to its unique structural features, 2-(3-(TrifluoroMethyl)phenylsulfonaMido)benzoic acid is also used as a valuable tool in the synthesis of new pharmaceutical compounds and bioactive molecules, contributing to the advancement of medicine and healthcare.
Check Digit Verification of cas no
The CAS Registry Mumber 306955-85-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,0,6,9,5 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 306955-85:
(8*3)+(7*0)+(6*6)+(5*9)+(4*5)+(3*5)+(2*8)+(1*5)=161
161 % 10 = 1
So 306955-85-1 is a valid CAS Registry Number.
306955-85-1Relevant academic research and scientific papers
Deoxygenative Arylation of Carboxylic Acids by Aryl Migration
Ruzi, Rehanguli,Ma, Junyang,Yuan, Xiang-Ai,Wang, Wenliang,Wang, Shanshan,Zhang, Muliang,Dai, Jie,Xie, Jin,Zhu, Chengjian
supporting information, p. 12724 - 12729 (2019/11/05)
An unprecedented deoxygenative arylation of aromatic carboxylic acids has been achieved, allowing the construction of an enhanced library of unsymmetrical diaryl ketones. The synergistic photoredox catalysis and phosphoranyl radical chemistry allows for precise cleavage of a stronger C?O bond and formation of a weaker C?C bond by 1,5-aryl migration under mild reaction conditions. This new protocol is independent of substrate redox-potential, electronic, and substituent effects. It affords a general and promising access to 60 examples of synthetically versatile o-amino and o-hydroxy diaryl ketones under redox-neutral conditions. Furthermore, it also brings one concise route to the total synthesis of quinolone alkaloid, (±)-yaequinolone A2, and a viridicatin derivative in satisfying yields.
