51979-87-4 Usage
Description
L-Valine, N-[[(4-nitrophenyl)methoxy]carbonyl]is a chemical compound that consists of an essential amino acid, L-Valine, and a carbonyl group attached to a nitrophenyl moiety. L-Valine, N-[[(4-nitrophenyl)methoxy]carbonyl]is significant for its role in protein synthesis and maintaining muscle tissue, as well as its potential applications in biochemical, pharmaceutical, or organic synthesis fields due to the presence of the carbonyl group and the nitrophenyl moiety.
Uses
Used in Biochemical Applications:
L-Valine, N-[[(4-nitrophenyl)methoxy]carbonyl]is used as a biochemical reagent for its ability to participate in various chemical reactions and processes, particularly due to the presence of the L-Valine amino acid and the carbonyl group.
Used in Pharmaceutical Applications:
In the pharmaceutical industry, L-Valine, N-[[(4-nitrophenyl)methoxy]carbonyl]is used as an intermediate in the synthesis of drugs, leveraging its unique structure to create new compounds with potential therapeutic effects.
Used in Organic Synthesis:
L-Valine, N-[[(4-nitrophenyl)methoxy]carbonyl]is utilized as a building block in organic synthesis, where the carbonyl group and the nitrophenyl moiety can be manipulated to form a variety of complex organic molecules for different applications.
Check Digit Verification of cas no
The CAS Registry Mumber 51979-87-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,9,7 and 9 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 51979-87:
(7*5)+(6*1)+(5*9)+(4*7)+(3*9)+(2*8)+(1*7)=164
164 % 10 = 4
So 51979-87-4 is a valid CAS Registry Number.
51979-87-4Relevant articles and documents
Reduction and pH dual-responsive block copolymers containing pendent p-nitrobenzyl carbamate functionalities: Synthesis and self-assembly behavior
Hu, Cong,Dong, Bingyang,Liu, Li
, p. 1333 - 1343 (2019)
We report on the preparation of reduction-responsive amphiphilic block copolymers containing pendent p-nitrobenzyl carbamate (pNBC)-caged primary amine moieties by reversible addition–fragmentation chain transfer (RAFT) radical polymerization using a poly
Nitrobenzyl esters as potential conjugated alkylating and differentiation promoting agents: Antitumor effect in vivo
Wakselman,Cerutti,Chany
, p. 519 - 526 (2007/10/02)
A series of ortho and para-nitrobenzyl esters of short chain fatty acids (C2 to C5) and of the lipophilic aminoacid, L-valine, and some other o-nitrobenzylated products were prepared. Bioreductive or hydrolytic cleavages of these compounds could release both differentiation promoting agents such as butyric acid and electrophilic moieties able to alkylate DNA. The antitumor effects of these compounds, either alone and/or associated with an immunostimulating agent (corynebacterium parvum, CP) or interferon (IFN) treatment, was studied using the 180 TG Crocker Sarcoma grafted onto Swiss mice. Based on the mean survival time and the final survival rate, the most active compounds used alone were the o-nitrobenzyl acetate and the 0-nitrobenzyl butyrate. Previous stimulation of the immune competent cells by CP before antitumor treatment increased the efficiency of most of the nitrobenzylated derivatives studied. The association with IFN did not significantly improve the antitumor effect.
