4079-61-2

Usage

Uses

Used in Pharmaceutical Industry:
Dibenzyl 2-aminoSuccinate is used as a pharmaceutical intermediate for its potential therapeutic properties, particularly in the treatment of neurological disorders. Its ability to chelate metal ions may contribute to its therapeutic effects.
Used in Organic Synthesis:
In the field of organic synthesis, dibenzyl 2-aminoSuccinate is used as a versatile building block for the synthesis of various organic compounds. Its reactivity and functional groups make it a valuable component in the creation of complex organic molecules.
Used in Metal Complexation Reactions:
Dibenzyl 2-aminoSuccinate is used as a ligand in metal complexation reactions due to its ability to chelate metal ions. This property allows it to form stable complexes with various metal ions, which can be useful in a range of applications, including catalysis and the development of new materials.
Used in Research Applications:
In research settings, dibenzyl 2-aminoSuccinate is utilized for its potential to contribute to the understanding of metal ion interactions and the development of new therapeutic agents. Its diverse applications make it a valuable tool for scientists exploring various areas of chemistry and medicine.

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Relevant academic research and scientific papers

Ternary nylon-3 copolymers as host-defense peptide mimics: Beyond hydrophobic and cationic subunits

Host-defense peptides (HDPs) are produced by eukaryotes to defend against bacterial infection, and diverse synthetic polymers have recently been explored as mimics of these natural peptides. HDPs are rich in both hydrophobic and cationic amino acid residu

ANTIFOULING AGENT FOR UNDERWATER ADHERING ORGANISMS HAVING AMINO ACID ISONITRILE SKELETON

PROBLEM TO BE SOLVED: To provide a novel antifouling agent for underwater adhering organisms having excellent characteristics compared with well-known antifouling agents. SOLUTION: An antifouling agent for underwater adhering organisms comprises a compound represented by formula (I) or salt thereof, or solvate thereof, as an active ingredient. COPYRIGHT: (C)2015,JPO&INPIT

Enantioselective synthesis of 1,2,4-triazolines by chiral iron(ii)-complex catalyzed cyclization of α-isocyano esters and azodicarboxylates

Enantioselective cyclization of α-isocyano esters with azodicarboxylates catalyzed by FeII-N,N′-dioxide complexes has been developed. Under mild conditions, a variety of 1,2,4-triazoline derivatives was obtained in high yields and enantioselectivities.