10420-63-0 Usage
Uses
Used in Synthesis and Analysis of Peptides and Proteins:
N-(2,4-DINITROPHENYL)-L-ALANINE METHYL ESTER is used as a reagent for the synthesis and analysis of peptides and proteins, contributing to the understanding of their structures and functions.
Used in Spectrophotometric and Chromatographic Analysis:
In Analytical Chemistry, N-(2,4-DINITROPHENYL)-L-ALANINE METHYL ESTER is used as a reagent for spectrophotometric and chromatographic analysis, particularly for identifying and quantifying amino acids and peptides, due to the distinctive 2,4-dinitrophenyl group.
Used in Enzymatic Reaction Studies:
N-(2,4-DINITROPHENYL)-L-ALANINE METHYL ESTER is employed in the study of enzymatic reactions, providing insights into the mechanisms and kinetics of enzyme-catalyzed processes.
Used in Pharmaceutical and Bioactive Compound Development:
In the Pharmaceutical Industry, N-(2,4-DINITROPHENYL)-L-ALANINE METHYL ESTER is used as a starting material or intermediate in the development of pharmaceuticals and bioactive compounds, leveraging its chemical properties for potential therapeutic applications.
Safety Precautions:
N-(2,4-DINITROPHENYL)-L-ALANINE METHYL ESTER is known to be a skin and eye irritant, and it is essential to handle N-(2,4-DINITROPHENYL)-L-ALANINE METHYL ESTER with proper safety measures to minimize health risks.
Check Digit Verification of cas no
The CAS Registry Mumber 10420-63-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,4,2 and 0 respectively; the second part has 2 digits, 6 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 10420-63:
(7*1)+(6*0)+(5*4)+(4*2)+(3*0)+(2*6)+(1*3)=50
50 % 10 = 0
So 10420-63-0 is a valid CAS Registry Number.
InChI:InChI=1/C10H11N3O6/c1-6(10(14)19-2)11-8-4-3-7(12(15)16)5-9(8)13(17)18/h3-6,11H,1-2H3/t6-/m0/s1
10420-63-0Relevant academic research and scientific papers
Iron- or Zinc-Mediated Synthetic Approach to Enantiopure Dihydroquinoxalinones
Li, Dazhi,Ollevier, Thierry
, p. 1273 - 1280 (2019/01/04)
A general and efficient synthesis of enantiopure dihydroquinoxalinones has been developed using naturally occurring amino acids as starting materials. The reductive cyclization of N-(o-nitroaryl)amino esters was performed by using iron and zinc metal under mild conditions in a water/ethyl acetate mixture. The corresponding dihydroquinoxalinones were obtained in moderate to high yields and high enantiomeric purity, among which 7 new compounds were unprecedented in the literature.
Synthesis of o-Nitroarylamines via Ipso Nucleophilic Substitution of Sulfonic Acids
Manne, Srinivasa Rao,Chandra, Jyoti,Mandal, Bhubaneswar
supporting information, p. 636 - 639 (2019/01/21)
A mild, efficient, and eco-friendly method for the synthesis of o-nitroarylamine from o-nitroaryl sulfonic acid via ipso nucleophilic aryl substitution by amine is described. The products have been obtained with good yields at room temperature without the assistance of any metal, activating agent, or toxic oxidant. This method is useful for racemization-free synthesis of N-aryl amino acid esters.
