1115-78-2 Usage
Description
H-D-ALA-ALA-OH, also known as D-Alanyl-Alanine, is a dipeptide consisting of two D-Alanine molecules joined by a peptide bond. It is an essential organic compound in biochemical and molecular biology research, playing a significant role in metabolic processes and peptide synthesis.
Used in Biochemistry and Molecular Biology Research:
H-D-ALA-ALA-OH is used as a research compound for studying peptide synthesis, exploring the health benefits of peptides, and understanding cell regulation and signaling mechanisms.
Used in Pharmaceutical Industry:
H-D-ALA-ALA-OH is used as a building block in the development of peptide-based drugs, targeting various therapeutic applications due to its role in metabolic processes and cell signaling.
Used in Nutritional Supplements:
H-D-ALA-ALA-OH is used as an ingredient in nutritional supplements to support overall health and well-being, given its essential role in the body's metabolic functions.
Used in Cosmetics Industry:
H-D-ALA-ALA-OH is used as an active ingredient in cosmetic products for its potential skin health benefits, leveraging its role in cell regulation and signaling.
Check Digit Verification of cas no
The CAS Registry Mumber 1115-78-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,1,1 and 5 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1115-78:
(6*1)+(5*1)+(4*1)+(3*5)+(2*7)+(1*8)=52
52 % 10 = 2
So 1115-78-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H12N2O3/c1-3(7)5(9)8-4(2)6(10)11/h3-4H,7H2,1-2H3,(H,8,9)(H,10,11)/t3-,4?/m1/s1
1115-78-2Relevant articles and documents
The dimethylsulfoxonium methylide as unique reagent for the simultaneous deprotection of amino and carboxyl function of N-Fmoc-α-amino acid and N-Fmoc-peptide esters
Spinella, Mariagiovanna,De Marco, Rosaria,Belsito, Emilia L.,Leggio, Antonella,Liguori, Angelo
, p. 2010 - 2016 (2013/03/13)
The dimethylsulfoxonium methylide is described as a unique and useful reagent for the simultaneous deprotection of amino and carboxyl function of N-Fmoc-α-amino acid and N-Fmoc-peptide esters. The new methodology was applied successfully both to solution- and solid-phase peptide synthesis. The adopted methodology was extended successfully also to peptides containing amino acids bearing acid-sensitive protecting group in side chains. Furthermore no measurable epimerization was observed in the deprotection reaction of N-Fmoc-dipeptide methyl esters with dimethylsulfoxonium methylide.
