N-α-(t-Butoxycarbonyl)-β-styryl-L-alanine dicyclohexylammonium salt
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N-α-(t-Butoxycarbonyl)-β-styryl-L-alanine dicyclohexylammonium salt

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Category
BOC-Amino Acids
Catalog number
BAT-005053
CAS number
331730-11-1
Molecular Formula
C28H44N2O4
Molecular Weight
472.67
N-α-(t-Butoxycarbonyl)-β-styryl-L-alanine dicyclohexylammonium salt
IUPAC Name
N-cyclohexylcyclohexanamine;(E,2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-5-phenylpent-4-enoic acid
Synonyms
Boc-Ala(Styr)-OH DCHA; Boc-L-Styrylalanine-DCHA; Dicyclohexylamine(S)-2-((tert-butoxycarbonyl)amino)-5-phenylpent-4-enoate; Boc-L-Styrylalanine dicyclohexylamine salt; Boc-D-Styrylalanine-DCHA
Purity
≥ 95%
InChI
InChI=1S/C16H21NO4.C12H23N/c1-16(2,3)21-15(20)17-13(14(18)19)11-7-10-12-8-5-4-6-9-12;1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h4-10,13H,11H2,1-3H3,(H,17,20)(H,18,19);11-13H,1-10H2/b10-7+;/t13-;/m0./s1
InChI Key
XFECITMZVLWAJB-LIGCKOFKSA-N
Canonical SMILES
CC(C)(C)OC(=O)NC(CC=CC1=CC=CC=C1)C(=O)O.C1CCC(CC1)NC2CCCCC2

N-α-(t-Butoxycarbonyl)-β-styryl-L-alanine dicyclohexylammonium salt, a specialized compound with diverse applications in bioscientific and pharmaceutical, realms plays a pivotal role in various key applications, characterized by heightened perplexity and burstiness:

Peptide Synthesis: Embracing N-α-(t-Butoxycarbonyl)-β-styryl-L-alanine dicyclohexylammonium salt in peptide synthesis, scientists leverage its prowess as a protected amino acid derivative. The t-butoxycarbonyl (Boc) group stands as a shield for the alpha-amino group facilitating selective peptide bond formation with finesse. This compound streamlines the synthesis procedure elevating the purity and yield of the targeted peptides to unprecedented levels.

Drug Design and Development: Unveiling potential in the realm of pharmaceutical innovation, this compound serves as a cornerstone for designing and developing avant-garde drugs. By integrating it into peptide-based drug candidates, researchers unearth new avenues for therapeutic exploration enhancing drug stability and activity manifold. Its distinct chemical composition holds promise for crafting compounds with superior pharmacokinetic properties revolutionizing drug development paradigms.

Structural Biology: In the intricate domain of structural biology, N-α-(t-Butoxycarbonyl)-β-styryl-L-alanine dicyclohexylammonium salt emerges as an invaluable asset for dissecting protein-ligand interactions. Crafting peptides infused with this amino acid, researchers embark on journeys to unravel binding affinities and unveil molecular mechanisms with precision.

Molecular Recognition Studies: Transcending boundaries this specialized amino acid derivative becomes a cornerstone in delving into molecular recognition phenomena. By integrating it into synthetic receptors or sensors, scientists dive into atomic-level interactions between molecules unraveling the secrets of molecular dance with unparalleled scrutiny. These studies form the bedrock for sculpting biosensors diagnostic tools and targeted therapies that promise breakthroughs in personalized medicine.

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