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Sku CI04029_5_G
Chem Impex
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Product Information

Product Name
Boc-O-benzyl-L-tyrosine 4-nitrophenyl ester
Brand Name
Chem Impex
Product Number
04029
CAS
13512-59-9
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
13453746
IUPAC Name
(4-nitrophenyl) (2S)-2-(2-methylpropan-2-yl)oxycarbonylamino-3-(4-phenylmethoxyphenyl)propanoate
InChI Key
VTUXNRKFFGSUAE-DEOSSOPVSA-N
SMILES
CC(C)(C)OC(=O)NC@@H(CC1=CC=C(C=C1)OCC2=CC=CC=C2)C(=O)OC3=CC=C(C=C3)N+(=O)O-

Description

Boc-O-benzyl-L-tyrosine 4-nitrophenyl ester is widely utilized in research focused on:

Peptide Synthesis: This compound serves as a key building block in the synthesis of peptides, particularly in the development of biologically active compounds. Its protective groups facilitate selective reactions, making it easier to create complex structures.

Drug Development: In pharmaceutical research, it is used to create prodrugs that enhance the solubility and bioavailability of therapeutic agents. This can lead to more effective treatments with fewer side effects.

Bioconjugation: The compound is employed in bioconjugation processes, allowing researchers to attach biomolecules to drugs or imaging agents. This application is crucial in targeted drug delivery systems.

Fluorescent Labeling: It can be used to introduce fluorescent tags in molecular biology studies, aiding in the visualization of proteins and other biomolecules in live cells.

Research in Neuroscience: Due to its structural similarity to neurotransmitters, it is explored in studies related to neuropharmacology, helping to understand receptor interactions and signaling pathways.

References Data Source From Pubchem

Synthesis of stereoisomer analogs of the amino end sequence of human growth hormone releasing factor

Publication Name: Pharmaceutical Chemistry Journal
Publication Date: 2006-05
DOI: 10.1007/s11094-006-0109-4

Synthesis of structural analogs of the 1–4 somatoliberin fragment

Publication Name: Pharmaceutical Chemistry Journal
Publication Date: 2006-04
DOI: 10.1007/s11094-006-0095-6

The effect of modifications of the A5 and A19 amino acid residues on the biological activity of insulin. [Leu5-A] and [Phe19-A] sheep insulins

Publication Name: Journal of Protein Chemistry
Publication Date: 1983-04
DOI: 10.1007/bf01025378