42259-95-0 Usage
Uses
Used in Pharmaceutical Industry:
(2-OXO-PYRROLIDIN-3-YL)-CARBAMIC ACID BENZYL ESTER is used as a building block for the synthesis of various drugs due to its unique chemical structure and biological activities.
Used in Organic Synthesis:
(2-OXO-PYRROLIDIN-3-YL)-CARBAMIC ACID BENZYL ESTER is used as a reagent in organic synthesis, contributing to the development of new chemical compounds and materials.
Used in Drug Discovery and Development:
(2-OXO-PYRROLIDIN-3-YL)-CARBAMIC ACID BENZYL ESTER is used as a key intermediate in the production of pharmaceuticals and agrochemicals, playing a crucial role in the development of new medications and potential therapeutic agents.
Used in Research:
(2-OXO-PYRROLIDIN-3-YL)-CARBAMIC ACID BENZYL ESTER is used in research for its potential applications in drug discovery and development, as well as for further exploration of its biological activities and properties.
Check Digit Verification of cas no
The CAS Registry Mumber 42259-95-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,2,2,5 and 9 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 42259-95:
(7*4)+(6*2)+(5*2)+(4*5)+(3*9)+(2*9)+(1*5)=120
120 % 10 = 0
So 42259-95-0 is a valid CAS Registry Number.
42259-95-0Relevant academic research and scientific papers
Straightforward synthesis of a novel class of rigid bicyclic dipeptidomimetics from simple dipeptides: Fused imidazole amino acids
Haberhauer, Gebhard,Rominger, Frank
, p. 780 - 784 (2007/10/03)
A novel class of rigid bicyclic dipeptidomimetics consisting of fused imidazole amino acids is presented. Their straightforward synthesis was realized by using simple dipeptides consisting of a diamino acid and threonine as starting material.
SPONTANEOUS CYCLIZATION OF A CHAIN SHORTENED LYSINE ANALOG
Ranganathan, S.,Ranganathan, D.,Singh, W. P.
, p. 3111 - 3114 (2007/10/02)
The chain shortened analog of lysine, H2NCH2CH2CH(NHZ)COOR, generated from N-protected glutamine esters, undergoes spontaneous cyclization.The results show that amino acids having H2NCH2CH2 - side chains cannot be supported on tRNA and provides a rationale for keeping the amino group of lysine by as many as four methylenes away from the peptide backbone.In sharp contrast, in the peptide environment, H2NCH2CH2CH(NHZ)CONHCH(X)COOMe, this unit is stable, thus demonstrating that if they are post translationally created, can be present as viable side chains in proteins.
