199679-83-9 Usage
Uses
Used in Pharmaceutical Synthesis:
(R)-2-(4-Chloro-phenylamino)-butyric acid methyl ester is used as a building block for the development of various pharmaceuticals, leveraging its molecular structure to create compounds with potential therapeutic applications.
Used in Agrochemical Synthesis:
In the agrochemical industry, (R)-2-(4-Chloro-phenylamino)-butyric acid methyl ester is used as an intermediate in the synthesis of compounds designed to protect crops and enhance agricultural productivity.
Used in Medicinal Chemistry Research:
(R)-2-(4-Chloro-phenylamino)-butyric acid methyl ester serves as a valuable asset in medicinal chemistry research, where it is studied for its potential anti-inflammatory and analgesic properties, contributing to the advancement of new drug therapies.
Used in Drug Development:
(R)-2-(4-Chloro-phenylamino)-butyric acid methyl ester is utilized in drug development due to its potential interactions with biological systems, which may lead to the creation of novel drugs with improved efficacy and safety profiles.
Check Digit Verification of cas no
The CAS Registry Mumber 199679-83-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,9,6,7 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 199679-83:
(8*1)+(7*9)+(6*9)+(5*6)+(4*7)+(3*9)+(2*8)+(1*3)=229
229 % 10 = 9
So 199679-83-9 is a valid CAS Registry Number.
199679-83-9Relevant academic research and scientific papers
Isosteres of chiral clofibric acid analogs: Synthesis, resolution, absolute configuration and HPLC detection of the optical purity
Ferorelli,Loiodice,Tortorella,Amoroso,Bettoni,Conte- Camerino,De Luca
, p. 367 - 374 (2007/10/03)
Both racemic and enantiomeric forms of some isosteres of chiral clofibric acid analogs have been synthesized. Also, the absolute configuration has been established by chemical correlation and the optical purity determined by a simple HPLC procedure. Moreover, these studies show that the isosteric substitution of the ether oxygen atom of α-aryloxy- alkanoic acids with sulfur, amino and methylene groups lead to compounds in which both biological activity and stereoselectivity regarding chloride channel are highly reduced.
