199679-83-9 Usage
General Description
The chemical (R)-2-(4-Chloro-phenylamino)-butyric acid methyl ester is a specific compound with a molecular structure consisting of a butyric acid chain attached to a 4-chloro-phenylamino group. It is typically used as a building block or intermediate in the synthesis of various pharmaceuticals and agrochemicals. (R)-2-(4-Chloro-phenylamino)-butyric acid methyl ester is known for its potential therapeutic properties and has been studied for its potential use as an anti-inflammatory and analgesic agent. Additionally, its structure suggests that it may have interactions with biological systems that could be beneficial for the development of new drugs. The methyl ester group allows for easier handling and manipulation of the compound in laboratory settings. Overall, (R)-2-(4-Chloro-phenylamino)-butyric acid methyl ester is a valuable chemical for medicinal chemistry research and drug development.
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 articles and documents
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.
