109745-84-8 Usage
Uses
Used in Pharmaceutical Applications:
L-Leucine, N-[N-(triphenylmethyl)-L-valyl]-, methyl ester is used as a building block for the synthesis of peptides and peptide analogues, which are essential in the development of new drugs and therapies.
Used in Research Applications:
L-Leucine, N-[N-(triphenylmethyl)-L-valyl]-, methyl ester serves as a valuable research tool for studying the properties and functions of L-leucine and its derivatives, as well as their interactions with other biomolecules.
Used in Sports Supplements Industry:
L-Leucine, N-[N-(triphenylmethyl)-L-valyl]-, methyl ester is used as an ingredient in sports supplements and muscle-building products due to its role in protein synthesis and muscle repair, contributing to enhanced athletic performance and muscle growth.
Used in Medical Applications:
The modified properties of L-Leucine, N-[N-(triphenylmethyl)-L-valyl]-, methyl ester may offer potential therapeutic benefits in specific medical conditions, making it a candidate for further exploration and development in the medical field.
Check Digit Verification of cas no
The CAS Registry Mumber 109745-84-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,9,7,4 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 109745-84:
(8*1)+(7*0)+(6*9)+(5*7)+(4*4)+(3*5)+(2*8)+(1*4)=148
148 % 10 = 8
So 109745-84-8 is a valid CAS Registry Number.
109745-84-8Relevant academic research and scientific papers
Amino Acids and Peptides, 63. - Peptide Synthesis via N- or O-Activation of Amino Acids with 1,2-Dihydro-4,6-dimethyl-2-thioxo-3-pyridinecarbonitrile. - Synthesis of the 8-11 Tetrapeptide Sequence of Cyclosporin
Schmidt, Ulrich,Potzolli, Bernd
, p. 935 - 942 (2007/10/02)
Peptides and N-methyl peptides have been prepared in high yields and nearly free of racemisation via N-activation (Scheme 1) or O-activation (Scheme 2) of N-acylamino acids and N-acyl-N-methylamino acids, respectively, by 1,2-dihydro-4,6-dimethyl-2-thioxo
