1245613-20-0 Usage
Uses
Used in Pharmaceutical Industry:
(S)-2-benzyloxycarbonylaminopentanedioic acid 1-allyl ester 5-ethyl ester is used as an intermediate in the synthesis of complex pharmaceutical compounds due to its multiple functional groups and reactivity.
Used in Chemical Synthesis:
In the chemical synthesis industry, (S)-2-benzyloxycarbonylaminopentanedioic acid 1-allyl ester 5-ethyl ester is used as a versatile building block for creating a variety of complex molecules, taking advantage of its diverse functional groups and reactivity.
Used in Research and Development:
(S)-2-benzyloxycarbonylaminopentanedioic acid 1-allyl ester 5-ethyl ester is utilized as a research compound for studying the properties and potential applications of compounds with multiple functional groups, contributing to the advancement of chemical knowledge and innovation.
Used in Material Science:
In the field of material science, (S)-2-benzyloxycarbonylaminopentanedioic acid 1-allyl ester 5-ethyl ester can be used as a precursor for developing new materials with specific properties, such as polymers with tailored characteristics or novel catalysts for various reactions.
Check Digit Verification of cas no
The CAS Registry Mumber 1245613-20-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,4,5,6,1 and 3 respectively; the second part has 2 digits, 2 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1245613-20:
(9*1)+(8*2)+(7*4)+(6*5)+(5*6)+(4*1)+(3*3)+(2*2)+(1*0)=130
130 % 10 = 0
So 1245613-20-0 is a valid CAS Registry Number.
1245613-20-0Relevant articles and documents
Bacillus subtilis esterase (BS2) and its double mutant have different selectivity in the removal of carboxyl protecting groups
Barbayianni, Efrosini,Kokotos, Christoforos G.,Bartsch, Sebastian,Drakou, Christina,Bornscheuer, Uwe T.,Kokotos, George
experimental part, p. 2325 - 2332 (2009/12/28)
An esterase from Bacillus subtilis (BS2) and its double mutant E188W/M193C quickly hydrolyze n-butyl, n-propyl, methoxyethyl and allyl esters. The wild-type BS2 preferentially removes such esters from the y-position of glutamate diesters, while the engineered enzyme has a reversed selectivity removing esters from the a-position of glutamate diesters. Automated docking and molecular dynamic simulations were performed to understand the molecular reason for the different regioselectivity.
