Product Added to Cart!
$299.20

FREE
SHIPPING

100% MONEY
BACK GUARANTEE

ONLINE
SUPPORT 24/7

Available on backorder. Please allow 2-3 weeks for production.
Sku CI03735_5_G
Chem Impex
Get Bulk Quote

Product Information

Product Name
Fmoc-O-tert-butyl-L-serine 3,4-dihydro-3-hydroxy-4-oxo-1,2,3-benzotriazine ester
Brand Name
Chem Impex
Product Number
03735
CAS
109434-27-7
Certificate of Analysis (COA)​
COA not found

General Information

PubChem CID
14189495
IUPAC Name
(4-oxo-1,2,3-benzotriazin-3-yl) (2S)-2-(9H-fluoren-9-ylmethoxycarbonylamino)-3-(2-methylpropan-2-yl)oxypropanoate
InChI Key
NCZXTUHFIKZNNH-VWLOTQADSA-N
SMILES
CC(C)(C)OCC@@H(C(=O)ON1C(=O)C2=CC=CC=C2N=N1)NC(=O)OCC3C4=CC=CC=C4C5=CC=CC=C35

Description

Fmoc-O-tert-butyl-L-serine 3,4-dihydro-3-hydroxy-4-oxo-1,2,3-benzotriazine ester is widely utilized in research focused on:

Peptide Synthesis: This compound serves as a protecting group in the synthesis of peptides, allowing for selective reactions and enhancing the overall yield and purity of the final product.

Drug Development: Its unique structure makes it valuable in the design of novel pharmaceuticals, particularly in targeting specific biological pathways, which can lead to more effective treatments.

Bioconjugation: It is used in bioconjugation processes to attach biomolecules to drugs or imaging agents, improving their stability and bioavailability in therapeutic applications.

Research in Biochemistry: This compound aids in studying protein interactions and functions, providing insights that are crucial for understanding cellular processes and disease mechanisms.

Material Science: Its properties can be exploited in the development of new materials, such as polymers, that have specific functionalities for applications in electronics and coatings.

References Data Source From Pubchem

ADP-ribosylation of alpha-Gi proteins by pertussis toxin. Positional dissection of acceptor sites using membrane anchored synthetic peptides

Publication Name: Methods in molecular biology (Clifton, N.J.)
Publication Date: 2000
DOI: 10.1385/1-59259-052-7:203