127127-26-8 Usage
Description
DL-2-(TRIFLUOROMETHYL)NORLEUCINE is a chemical compound that is part of the norleucine derivatives class. It is an unnatural amino acid and a structural analog of leucine, with a trifluoromethyl group attached to the norleucine molecule. This trifluoromethyl group endows it with unique physicochemical properties, which make it valuable for various applications in the fields of medicinal and pharmaceutical chemistry.
Uses
Used in Pharmaceutical Industry:
DL-2-(TRIFLUOROMETHYL)NORLEUCINE is used as a building block for the synthesis of peptide-based drugs. Its unique properties allow for the creation of novel pharmaceutical compounds with potential therapeutic applications.
Used in Medicinal Chemistry Research:
DL-2-(TRIFLUOROMETHYL)NORLEUCINE is utilized as a tool in chemical biology research. Its synthetic accessibility and versatile chemical reactivity make it a valuable component in the development of new drugs and understanding biological processes.
Used in Antimicrobial Agent Development:
DL-2-(TRIFLUOROMETHYL)NORLEUCINE has been studied for its potential use in the development of antimicrobial agents. Its unique structure and properties may contribute to the creation of new antimicrobial compounds to combat resistant pathogens.
Check Digit Verification of cas no
The CAS Registry Mumber 127127-26-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,7,1,2 and 7 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 127127-26:
(8*1)+(7*2)+(6*7)+(5*1)+(4*2)+(3*7)+(2*2)+(1*6)=108
108 % 10 = 8
So 127127-26-8 is a valid CAS Registry Number.
127127-26-8Relevant articles and documents
Homologation of trifluoroacetimidoyl iodides by palladium-catalyzed carbonylation. An approach to α-amino perfluoroalkanoic acids
Watanabe,Hashizume,Uneyama
, p. 4333 - 4336 (2007/10/02)
Homologation of trifluoroacetimidoyl iodides and the related perfluoro-compounds by palladium-catalyst under CO(1atm)-atmosphere in the presence of alcohols gives α-imino perfluoroalkanoates which are transformed to α-amino perfluoroalkanoic acids.
