240490-00-0 Usage
Uses
Used in Pharmaceutical Industry:
AMINO-(2-TRIFLUOROMETHYL-PHENYL)-ACETIC ACID is utilized as a key intermediate in the synthesis of potential drug candidates. Its unique structure allows for the development of new therapeutic agents with specific biological activities.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, AMINO-(2-TRIFLUOROMETHYL-PHENYL)-ACETIC ACID serves as a valuable compound for research. It is employed in the exploration of novel chemical entities and their interactions with biological targets, contributing to the advancement of our understanding of disease mechanisms and the design of effective treatments.
Used in Drug Discovery and Development:
AMINO-(2-TRIFLUOROMETHYL-PHENYL)-ACETIC ACID's unique properties make it a promising candidate for drug discovery and development. Its potential therapeutic applications are currently being studied for the treatment of various diseases, highlighting its versatility and importance in the pharmaceutical sector.
Check Digit Verification of cas no
The CAS Registry Mumber 240490-00-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,4,0,4,9 and 0 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 240490-00:
(8*2)+(7*4)+(6*0)+(5*4)+(4*9)+(3*0)+(2*0)+(1*0)=100
100 % 10 = 0
So 240490-00-0 is a valid CAS Registry Number.
InChI:InChI=1/C9H8F3NO2/c10-9(11,12)6-4-2-1-3-5(6)7(13)8(14)15/h1-4,7H,13H2,(H,14,15)/t7-/m0/s1
240490-00-0Relevant academic research and scientific papers
Synthesis of Unprotected 2-Arylglycines by Transamination of Arylglyoxylic Acids with 2-(2-Chlorophenyl)glycine
Inada, Haruki,Shibuya, Masatoshi,Yamamoto, Yoshihiko
, p. 11047 - 11059 (2020/10/12)
The transamination of α-keto acids with 2-phenylglycine is an effective methodology for directly synthesizing unprotected α-amino acids. However, the synthesis of 2-arylglycines by transamination is problematic because the corresponding products, 2-arylglycines, transaminate the starting arylglyoxylic acids. Herein, we demonstrate the use of commercially available l-2-(2-chlorophenyl)glycine as the nitrogen source in the transamination of arylglyoxylic acids, producing the corresponding 2-arylglycines without interference from the undesired self-transamination process.
