Boc-3-(9-anthryl)-L-alanine
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Boc-3-(9-anthryl)-L-alanine

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Category
BOC-Amino Acids
Catalog number
BAT-007970
CAS number
332065-09-5
Molecular Formula
C22H23NO4
Molecular Weight
365.42
Boc-3-(9-anthryl)-L-alanine
IUPAC Name
(2S)-3-anthracen-9-yl-2-[(2-methylpropan-2-yl)oxycarbonylamino]propanoic acid
Synonyms
Boc-3-Ala(9-anthryl)-OH; (S)-3-(Anthracen-9-yl)-2-((tert-butoxycarbonyl)amino)propanoic acid; BOC-L-9-ANTHRYLALANINE; Boc-L-Anthrylalanine; Boc-Ala(9-Anth)-OH; N-alpha-(t-Butoxycarbonyl)-beta-(9-anthryl)-L-alanine; (2S)-3-(9-ANTHRYL)-2-[(TERT-BUTOXY)CARBONYLAMINO]PROPANOIC ACID
Purity
99%
Density
1.230±0.06 g/cm3 (Predicted)
Boiling Point
589.9±43.0 °C (Predicted)
Storage
Store at 2-8 °C
InChI
InChI=1S/C22H23NO4/c1-22(2,3)27-21(26)23-19(20(24)25)13-18-16-10-6-4-8-14(16)12-15-9-5-7-11-17(15)18/h4-12,19H,13H2,1-3H3,(H,23,26)(H,24,25)/t19-/m0/s1
InChI Key
GYXDEFFXDFOZMJ-IBGZPJMESA-N
Canonical SMILES
CC(C)(C)OC(=O)NC(CC1=C2C=CC=CC2=CC3=CC=CC=C31)C(=O)O

Boc-3-(9-anthryl)-L-alanine, a synthetic amino acid derivative, exhibits diverse applications in both research and industry. Here are the key applications highlighted with a high degree of perplexity and burstiness:

Peptide Synthesis: A cornerstone in the realm of peptide synthesis, Boc-3-(9-anthryl)-L-alanine serves as a pivotal building block for crafting fluorescent peptides. By integrating this derivative into peptide sequences, researchers delve into the intricacies of protein-protein interactions using fluorescence spectroscopy. This methodology plays a critical role in unraveling the enigmatic web of biological interactions at a minute molecular level.

Drug Development: At the forefront of drug discovery, Boc-3-(9-anthryl)-L-alanine emerges as a valuable tool for scrutinizing enzyme-substrate interactions. The anthryl group facilitates the monitoring and tracking of biochemical processes through fluorescence aiding in the identification of potential inhibitors and fine-tuning lead compounds essential for forging new therapeutic agents.

Biophysical Studies: Delving into the realm of biophysical research, Boc-3-(9-anthryl)-L-alanine finds its niche in studying membrane dynamics and protein folding. Leveraging its fluorescent attributes scientists probe into the structural alterations and behaviors of biomolecules across diverse environments. This endeavor is pivotal in decoding the underlying principles of molecular biology and biochemistry shedding light on the intricate dance of biomolecular interactions.

Environmental Monitoring: In the arena of environmental sciences, this compound emerges as a potent tool for detecting pollutants and toxins. The fluorescence of Boc-3-(9-anthryl)-L-alanine responds sensitively to the presence of specific contaminants offering a foundation for precision monitoring assays. This capability aids in accurate assessment of environmental health and safety bolstering efforts to safeguard our ecosystems effectively.

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