54895-27-1 Usage
Description
D-2-tert-butoxycarbonylamino-2-(3-nitrophenyl)-acetic acid, also known as Boc-Gly-(3-nitro-L-tyrosine)-OH, is a chemical compound that serves as a building block in the synthesis of peptides and proteins. It is a derivative of glycine and 3-nitro-L-tyrosine, characterized by its white crystalline powder form and stability under normal conditions. D-2-tert-butoxycarbonylamino-2-(3-nitrophenyl)-acetic acid plays a pivotal role in biochemistry and pharmaceutical research, particularly in the development of new drugs and the study of biological processes involving peptides and proteins.
Uses
Used in Pharmaceutical Research:
D-2-tert-butoxycarbonylamino-2-(3-nitrophenyl)-acetic acid is utilized as a key component in the synthesis of peptides and proteins for pharmaceutical research. It aids in the development of new drugs and treatments by enabling the creation of complex peptide structures that can be tested for therapeutic efficacy.
Used in Biochemical Studies:
In the field of biochemistry, D-2-tert-butoxycarbonylamino-2-(3-nitrophenyl)-acetic acid is employed as a research tool to study biological processes that involve peptides and proteins. Its incorporation into these biomolecules allows scientists to investigate their functions, interactions, and mechanisms within biological systems.
Used in Drug Development:
D-2-tert-butoxycarbonylamino-2-(3-nitrophenyl)-acetic acid is used as a building block in drug development for the creation of novel therapeutic agents. Its ability to form stable peptide bonds makes it a valuable asset in the design and synthesis of potential new drugs that target specific biological pathways or diseases.
Used in Peptide Synthesis:
D-2-tert-butoxycarbonylamino-2-(3-nitrophenyl)-acetic acid is used as a reactant in peptide synthesis, allowing for the assembly of custom peptides with specific sequences and functionalities. These peptides can be used for a variety of applications, including as therapeutic agents, research tools, or components of drug delivery systems.
Used in Protein Engineering:
In protein engineering, D-2-tert-butoxycarbonylamino-2-(3-nitrophenyl)-acetic acid is used to modify or create new proteins with desired properties. This can involve altering protein structure, stability, or function, which can lead to the development of improved enzymes, vaccines, or other biotherapeutic agents.
Check Digit Verification of cas no
The CAS Registry Mumber 54895-27-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,4,8,9 and 5 respectively; the second part has 2 digits, 2 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 54895-27:
(7*5)+(6*4)+(5*8)+(4*9)+(3*5)+(2*2)+(1*7)=161
161 % 10 = 1
So 54895-27-1 is a valid CAS Registry Number.
54895-27-1Relevant articles and documents
Novel carboxaldehyde mediated synthetic pathway for 5′-amino adenosine analogues
Gibbons, Garrett S.,Showalter, Hollis D.,Nikolovska-Coleska, Zaneta
, p. 348 - 360 (2015/05/05)
Modifications of the 5′-position of adenosine have been prepared via a novel 5′-carboxaldehyde synthon. The described methodology should prove useful for making related compounds in which amine-derived moieties off the 5′-position of adenosine (or related nucleoside congeners) can be easily incorporated via reductive amination, especially for the incorporation of aromatic amines.
α-amino-α-(ureidophenyl)acetamidocephalosporins
-
, (2008/06/13)
Cephalosporins with a α-amino-(ureidophenyl)acetamido substituent at position 7 are prepared by acylation of a 7-aminocephalosporin with a derivative of α-amino-p(or m)-ureidophenylacetic acid. These compounds are antibacterial agents.
