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Chem Impex
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Product Information

Product Name
Z-S-benzyl-L-cysteine 4-nitrophenyl ester
Brand Name
Chem Impex
Product Number
02153
CAS
3401-37-4
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
294945
IUPAC Name
(4-nitrophenyl) 3-benzylsulfanyl-2-(phenylmethoxycarbonylamino)propanoate
InChI Key
LQPKVCBYFUURJM-UHFFFAOYSA-N
SMILES
C1=CC=C(C=C1)COC(=O)NC(CSCC2=CC=CC=C2)C(=O)OC3=CC=C(C=C3)N+(=O)O-

Application

Z-S-benzyl-L-cysteine 4-nitrophenyl ester is widely utilized in research focused on:

Drug Development: This compound serves as a valuable intermediate in the synthesis of pharmaceuticals, particularly in the development of drugs targeting various diseases, including cancer and neurological disorders.

Bioconjugation: It is employed in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, enhancing the delivery and efficacy of therapeutic agents.

Analytical Chemistry: The compound is used in analytical methods for detecting and quantifying specific biomolecules, providing essential data for research and quality control in laboratories.

Peptide Synthesis: It plays a crucial role in peptide synthesis, particularly in the formation of complex peptides that can be used in vaccines or as therapeutic agents.

Research on Antioxidants: This compound is studied for its potential antioxidant properties, contributing to research aimed at developing new antioxidants for health and wellness applications.

References Data Source From Pubchem

9-Fluorenylmethyl chloroformate (Fmoc-Cl) as a useful reagent for the synthesis of pentafluorophenyl, 2,4,5-trichlorophenyl, pentachlorophenyl, p-nitrophenyl, o-nitrophenyl and succinimidyl esters of N -urethane protected amino acids

Publication Name: International Journal of Peptide Research and Therapeutics
Publication Date: 2003-11
DOI: 10.1007/bf02442600|10.1007/s10989-005-3968-8|10.1023/b:lips.0000049132.01206.4c

[On peptide syntheses. XLIV. Synthesis of ser4-glu(NH2)8-oxytocin (glumitocin)]

Publication Name: Experientia
Publication Date: 1968-01-15
DOI: 10.1007/bf02136762