112674-65-4 Usage
Uses
Used in Pharmaceutical Industry:
L-Leucine, N-acetyl-4-methylis used as a building block for the synthesis of peptides and pharmaceuticals, due to its structural properties derived from the essential amino acid leucine.
Used in Anti-inflammatory Applications:
L-Leucine, N-acetyl-4-methylis used as an anti-inflammatory agent for its potential to reduce inflammation, which is beneficial in treating conditions characterized by inflammatory responses.
Used in Antioxidant Applications:
L-Leucine, N-acetyl-4-methylis used as an antioxidant, leveraging its potential to neutralize harmful free radicals, thereby protecting the body from oxidative stress and related disorders.
Used in Metabolic and Neurological Disorder Treatment:
L-Leucine, N-acetyl-4-methylis used as a therapeutic agent in the treatment of metabolic and neurological disorders, owing to its potential role in managing these conditions.
Used in Drug Development:
L-Leucine, N-acetyl-4-methylis used as a component in the development of new drugs for various medical conditions, given its diverse biological activities and potential health benefits.
Check Digit Verification of cas no
The CAS Registry Mumber 112674-65-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,6,7 and 4 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 112674-65:
(8*1)+(7*1)+(6*2)+(5*6)+(4*7)+(3*4)+(2*6)+(1*5)=114
114 % 10 = 4
So 112674-65-4 is a valid CAS Registry Number.
112674-65-4Relevant academic research and scientific papers
PEPTIDES CONTAINING A NEOPENTYLGLYCINE RESIDUE
Pospisek, Jan,Blaha, Karel
, p. 514 - 521 (2007/10/02)
Neopentylglycine (III, 2-amino-4,4-dimethylpentanoic acid) was synthesized in both enantiomeric forms.Using the conventional methods of peptide synthesis, L-prolyl-L-neopentylglycylglycine amide (VII), the diastereomeric cyclodipeptides cyclo(L-neopentylglycyl-L-prolyl) (IXa) and cyclo(D-neopentylglycyl-L-prolyl) (IXb) and also N-acetyl-L-neopentylglycine methylamide (X) were prepared as models for further studies on physical properties and conformation of peptides.
