N-α-(t-Butoxycarbonyl)-D-asparagine 4-nitrophenyl ester
Need Assistance?
  • US & Canada:
    +
  • UK: +

N-α-(t-Butoxycarbonyl)-D-asparagine 4-nitrophenyl ester

* Please kindly note that our products are not to be used for therapeutic purposes and cannot be sold to patients.

Category
BOC-Amino Acids
Catalog number
BAT-003094
CAS number
104199-82-8
Molecular Formula
C15H19N3O7
Molecular Weight
353.33
N-α-(t-Butoxycarbonyl)-D-asparagine 4-nitrophenyl ester
IUPAC Name
(4-nitrophenyl) (2R)-4-amino-2-[(2-methylpropan-2-yl)oxycarbonylamino]-4-oxobutanoate
Synonyms
Boc-D-Asn-ONp; N-PYRIDIN-3-YLPROPANE-1,3-DIAMINE; N1-pyridin-3-yl-propane-1,3-diamine; N1-t-boc C1-p-nitrophenol asparagine
Purity
≥ 95%
Density
1.318 g/cm3
Boiling Point
609.3 °C at 760 mmHg
Storage
Store at -20 °C
InChI
InChI=1S/C15H19N3O7/c1-15(2,3)25-14(21)17-11(8-12(16)19)13(20)24-10-6-4-9(5-7-10)18(22)23/h4-7,11H,8H2,1-3H3,(H2,16,19)(H,17,21)/t11-/m1/s1
InChI Key
IAPXDJMULQXGDD-LLVKDONJSA-N
Canonical SMILES
CC(C)(C)OC(=O)NC(CC(=O)N)C(=O)OC1=CC=C(C=C1)[N+](=O)[O-]

N-α-(t-Butoxycarbonyl)-D-asparagine 4-nitrophenyl ester, a specialized reagent with diverse applications in biochemistry and pharmaceuticals.

Peptide Synthesis: Playing a pivotal role in solid-phase peptide synthesis, N-α-(t-Butoxycarbonyl)-D-asparagine 4-nitrophenyl ester facilitates the incorporation of shielded D-asparagine residues into peptides. This process enables the exploration of structure-function relationships within proteins, ensuring precision and purity in synthetic peptides, crucial for biochemical investigations.

Proteomics Research: Within the realm of proteomics, this compound aids in generating peptide analogs and derivatives for various analytical methods. These peptides serve as standards in mass spectrometry analyses, shedding light on protein modifications and interactions. Through this application, researchers unravel complex protein networks and identify potential biomarkers, driving cutting-edge research.

Drug Development: Serving as a cornerstone in synthesizing therapeutic peptides and peptidomimetics, this compound offers high specificity and minimal toxicity, making it a promising asset in pharmaceutical advancement. Its role in peptide assembly supports the creation of innovative drugs, paving the way for potential breakthroughs in healthcare.

Enzyme Mechanism Studies: In enzyme assays, this compound plays a crucial role in exploring the specificity and catalytic mechanisms of proteases and peptidases. By mimicking substrates or inhibitors, it aids in elucidating enzyme kinetics and activity, contributing to a deeper understanding of enzyme functions and the development of enzyme inhibitors for therapeutic purposes.

Online Inquiry
Inquiry Basket