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Chem Impex
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Product Information

Product Name
Na-Boc-L-asparagine 4-nitrophenyl ester
Brand Name
Chem Impex
Product Number
01335
CAS
4587-33-1
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
439663
IUPAC Name
(4-nitrophenyl) (2S)-4-amino-2-(2-methylpropan-2-yl)oxycarbonylamino-4-oxobutanoate
InChI Key
IAPXDJMULQXGDD-NSHDSACASA-N
SMILES
CC(C)(C)OC(=O)NC@@H(CC(=O)N)C(=O)OC1=CC=C(C=C1)N+(=O)O-

Application

Na-Boc-L-asparagine 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, allowing researchers to create complex molecules for drug development and biological studies.

Bioconjugation: It is used in bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules, enhancing the functionality of drugs and diagnostics.

Fluorescent Probes: The ester can be modified to create fluorescent probes, which are essential in imaging techniques for studying cellular processes in real-time.

Enzyme Inhibition Studies: Researchers utilize this compound to investigate enzyme activity and inhibition, providing insights into metabolic pathways and potential therapeutic targets.

Drug Delivery Systems: Its unique properties make it suitable for developing advanced drug delivery systems, improving the efficiency and specificity of therapeutic agents.

References Data Source From Pubchem

The total large-scale synthesis of argiopine

Publication Name: Russian Journal of Bioorganic Chemistry
Publication Date: 2009-11
DOI: 10.1134/s1068162009060120

The Role of the Merrifield Solid Phase Method in the Discovery and Exploration of a New Class of Selective Vasopressin Hypotensive Agonists

Publication Name: International Journal of Peptide Research and Therapeutics
Publication Date: 2007-03-10
DOI: 10.1007/s10989-007-9089-9

The hydrolysis of primary amide groups in Asn/Gln-containing peptides

Publication Name: Russian Journal of Bioorganic Chemistry
Publication Date: 2000-06
DOI: 10.1007/bf02758662

Synthesis and disulfide structure determination of conotoxin GS, a γ-carboxyglutamic acid-containing neurotoxic peptide

Publication Name: International Journal of Peptide Research and Therapeutics
Publication Date: 1995-08
DOI: 10.1007/bf00122919

The semicarbazone dipeptide isostere in imino azapeptides: Synthesis and structure

Publication Name: Peptides 1994
Publication Date: 1995
DOI: 10.1007/978-94-011-1468-4_319