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Product Information

Product Name
Diphenylmethylene-glycine benzyl ester
Brand Name
Chem Impex
Product Number
31240
CAS
81477-91-0
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
11782449
IUPAC Name
benzyl 2-(benzhydrylideneamino)acetate
InChI Key
KFNIDRLZPBRDNJ-UHFFFAOYSA-N
SMILES
C1=CC=C(C=C1)COC(=O)CN=C(C2=CC=CC=C2)C3=CC=CC=C3

Application

Diphenylmethylene-glycine benzyl ester is widely utilized in research focused on:

Pharmaceutical Development: This compound serves as an important intermediate in synthesizing various pharmaceuticals, particularly in the development of analgesics and anti-inflammatory drugs.

Biochemical Research: It is used in studies exploring enzyme inhibition and protein interactions, aiding researchers in understanding biological pathways and disease mechanisms.

Organic Synthesis: The compound is a valuable reagent in organic chemistry for creating complex molecules, making it essential for chemists working on innovative material designs.

Cosmetic Formulations: Its properties allow it to be incorporated into cosmetic products, enhancing skin absorption and providing moisturizing benefits.

Agricultural Applications: This chemical can be used in developing agrochemicals, contributing to more effective pest control solutions that are safer for the environment.

References Data Source From Pubchem

Synthesis of Tricyclic Marine Alkaloids, Cylindricines, Lepadiformines, Fasicularin, and Polycitorols: A Recent Update

Publication Name: Synthesis
Publication Date: 2017-12-14
DOI: 10.1055/s-0036-1589521

Practical Methods for the Synthesis of Symmetrically α,α-Disubstituted α-Amino Acids

Publication Name: Synthesis
Publication Date: 2010-05-18
DOI: 10.1055/s-0029-1220013

Organocatalytic Enantioselective Michael and Hetero-Michael Reactions

Publication Name: Synthesis
Publication Date: 2007-07-03
DOI: 10.1055/s-2007-983747

Total Synthesis of (+)-Cylindricine C Using an Organocatalytic Michael Reaction

Publication Name: Synfacts
Publication Date: 2006-09
DOI: 10.1055/s-2006-949223