84787-81-5 Usage
Uses
Used in Organic Synthesis:
Ethyl N2-[(tert-butoxy)carbonyl]-L-argininate is used as a protecting group in organic synthesis for the guanidino group of arginine. This allows for selective reactions to occur at other sites on the molecule without affecting the guanidino group, facilitating the synthesis of complex organic compounds.
Used in Peptide Chemistry:
In peptide chemistry, ethyl N2-[(tert-butoxy)carbonyl]-L-argininate is utilized as a protecting group for the guanidino group of arginine during the synthesis of peptides. The Boc group can be removed under mild acidic conditions, enabling the formation of arginine-containing peptides with specific sequences and functions.
Used in Pharmaceutical Industry:
Ethyl N2-[(tert-butoxy)carbonyl]-L-argininate is used as an important intermediate in the synthesis of various bioactive molecules and pharmaceuticals. Its role in protecting the guanidino group of arginine during the synthesis process allows for the development of novel drugs with targeted therapeutic effects.
Used in the Preparation of Arginine-Containing Peptides and Peptidomimetics:
ethyl N2-[(tert-butoxy)carbonyl]-L-argininate is employed in the preparation of arginine-containing peptides and peptidomimetics, which are short protein-like molecules that mimic the structure and function of natural peptides. Ethyl N2-[(tert-butoxy)carbonyl]-L-argininate aids in the synthesis of these molecules, enabling the development of potential therapeutic agents with specific biological activities.
Check Digit Verification of cas no
The CAS Registry Mumber 84787-81-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,4,7,8 and 7 respectively; the second part has 2 digits, 8 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 84787-81:
(7*8)+(6*4)+(5*7)+(4*8)+(3*7)+(2*8)+(1*1)=185
185 % 10 = 5
So 84787-81-5 is a valid CAS Registry Number.
InChI:InChI=1/C13H26N4O4/c1-5-20-10(18)9(7-6-8-16-11(14)15)17-12(19)21-13(2,3)4/h9H,5-8H2,1-4H3,(H,17,19)(H4,14,15,16)/t9-/m0/s1
84787-81-5Relevant academic research and scientific papers
SYNTHESIS OF AMINO ACID ESTERS BY PAPAIN
Cantacuzene, D.,Pascal, F.,Guerreiro, C.
, p. 1823 - 1826 (2007/10/02)
A wide range of N-Boc-amino acid esters were synthesized from N-Boc-amino acids and alcohol using papain as catalyst.Suitable biphasic reaction mixtures were found for most amino acids to achieve high yield of ester synthesis.With N-Boc-L-aspartic and glutamic acids only the α carbonyl group esterified, without racemisation.
