124573-79-1 Usage
Uses
Used in Pharmaceutical Research:
(4-Fluoro-phenylamino)-phenyl-acetic acid is used as a key intermediate in the synthesis of various pharmaceutical drugs. Its unique structure allows for the development of novel drug candidates with potential therapeutic benefits.
Used in Organic Synthesis:
In the field of organic synthesis, (4-Fluoro-phenylamino)-phenyl-acetic acid serves as a valuable building block for the creation of more complex molecules. Its fluoro-phenylamino group can be further modified or used as a starting point for the synthesis of a wide range of organic compounds.
Used in Biochemistry and Medicinal Chemistry:
(4-Fluoro-phenylamino)-phenyl-acetic acid is employed as a research tool in biochemistry and medicinal chemistry. Its unique properties make it an important molecule for studying enzyme interactions, receptor binding, and other biological processes. Additionally, it can be used to develop new drugs targeting specific biological pathways.
Used in Drug Development:
In the pharmaceutical industry, (4-Fluoro-phenylamino)-phenyl-acetic acid is used as a starting material for the development of new drugs. Its potential therapeutic uses make it a valuable asset in the search for novel treatments for various diseases and conditions.
Check Digit Verification of cas no
The CAS Registry Mumber 124573-79-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,4,5,7 and 3 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 124573-79:
(8*1)+(7*2)+(6*4)+(5*5)+(4*7)+(3*3)+(2*7)+(1*9)=131
131 % 10 = 1
So 124573-79-1 is a valid CAS Registry Number.
124573-79-1Relevant academic research and scientific papers
A synthesis of α-amino acids via direct reductive carboxylation of imines with carbon dioxide
Sathe, Ajay A.,Hartline, Douglas R.,Radosevich, Alexander T.
, p. 5040 - 5042 (2013/06/05)
A method for the synthesis of α-amino acids by direct reductive carboxylation of aromatic imines with CO2 is described. The protocol employs readily available commercial reagents and serves as a one-step alternative to the Strecker synthesis. The Royal Society of Chemistry 2013.
Synthesis of Some New 3,4-Diarylsydnones
Csongar, Ch.,Mueller, I.,Slezak, H.,Klebsch, H.-J.,Tomaschewski, G.
, p. 1006 - 1014 (2007/10/02)
The synthesis of some new sydnones 4 is described.Their characteristic absorption maxima, mass spectroscopic fragmentation and C=O-valence vibrations are given.The sydnones 4 are synthezid by nitrosation of C,N-diarylglycines 3 (from strecker synthesis) a
