126829-54-7 Usage
Description
3-(2-NAPHTHYL)-L-ALANINE BENZYL ESTER 4-TOLUENESULFONATE SALT is a chemical compound that is commonly used in laboratories for various research and industrial purposes. It is a salt form of 3-(2-NAPHTHYL)-L-ALANINE BENZYL ESTER, which is an amino acid derivative. 3-(2-NAPHTHYL)-L-ALANINE BENZYL ESTER 4-TOLUENESULFONATE SALT is known for its stability, solubility in organic solvents, and versatility in scientific and industrial applications.
Used in Pharmaceutical Industry:
3-(2-NAPHTHYL)-L-ALANINE BENZYL ESTER 4-TOLUENESULFONATE SALT is used as a building block for the synthesis of peptides and other organic molecules, contributing to the development of new drugs and therapeutic agents.
Used in Chemical Research:
3-(2-NAPHTHYL)-L-ALANINE BENZYL ESTER 4-TOLUENESULFONATE SALT is used as a reagent in various chemical reactions, facilitating the synthesis of complex organic compounds and aiding in the advancement of chemical knowledge.
Used in Analytical Techniques:
3-(2-NAPHTHYL)-L-ALANINE BENZYL ESTER 4-TOLUENESULFONATE SALT is used as a component in chromatography and other analytical methods, enhancing the separation, identification, and quantification of compounds in various samples.
Check Digit Verification of cas no
The CAS Registry Mumber 126829-54-7 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,2,6,8,2 and 9 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 126829-54:
(8*1)+(7*2)+(6*6)+(5*8)+(4*2)+(3*9)+(2*5)+(1*4)=147
147 % 10 = 7
So 126829-54-7 is a valid CAS Registry Number.
126829-54-7Relevant articles and documents
Unusual reactivity of nitronates with an aryl alkyl carbonate: Synthesis of α-amino esters
Reddy, Golipalli Ramana,Mukherjee, Debopreeti,Chittoory, Arjun Kumar,Rajaram, Sridhar
, p. 5874 - 5877 (2015/01/08)
The monoanions of nitroalkanes are ambident nucleophiles that react with carbonate electrophiles through the oxygen atom. Products arising from reactivity at the carbon atom will yield α-nitro esters, which are precursors for α-amino esters. We demonstrate this in the reactions of nitroalkanes with benzyl phenyl carbonate and DABCO where α-nitro esters are obtained instead of nitrile oxides. The products are readily reduced to α-amino esters. This pathway could be a safe alternative to the Strecker reaction.
