Boc-β-(2-thienyl)-D-alanine dicyclohexylammonium salt
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Boc-β-(2-thienyl)-D-alanine dicyclohexylammonium salt

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Category
BOC-Amino Acids
Catalog number
BAT-007178
CAS number
78452-59-2
Molecular Formula
C12H17NO4S·C12H23N
Molecular Weight
452.65
Boc-β-(2-thienyl)-D-alanine dicyclohexylammonium salt
IUPAC Name
N-cyclohexylcyclohexanamine;(2R)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-thiophen-2-ylpropanoic acid
Synonyms
Boc-3-D-Ala(2-thienyl)-OH DCHA
Related CAS
78452-55-8 (free base)
Purity
≥ 99% (HPLC)
Melting Point
227-231 °C
Storage
Store at 2-8 °C
InChI
InChI=1S/C12H17NO4S.C12H23N/c1-12(2,3)17-11(16)13-9(10(14)15)7-8-5-4-6-18-8;1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h4-6,9H,7H2,1-3H3,(H,13,16)(H,14,15);11-13H,1-10H2/t9-;/m1./s1
InChI Key
HTHJUPIDDUMKSU-SBSPUUFOSA-N
Canonical SMILES
CC(C)(C)OC(=O)NC(CC1=CC=CS1)C(=O)O.C1CCC(CC1)NC2CCCCC2

Boc-β-(2-thienyl)-D-alanine dicyclohexylammonium salt, a specialized compound prevalent in biosciences and pharmaceutical research, showcases a diverse array of applications. Here are the key applications presented with a high degree of perplexity and burstiness:

Peptide Synthesis: Positioned as a fundamental component in solid-phase peptide synthesis, Boc-β-(2-thienyl)-D-alanine dicyclohexylammonium salt assumes a pivotal role in constructing peptides with precise sequences and tailored modifications. The strategic incorporation of the Boc protective group streamlines selective reactions crucial for fashioning intricate peptide architectures heralding a new era of sophistication in peptide design.

Drug Development: Embracing the cutting edge of pharmaceutical innovation, Boc-β-(2-thienyl)-D-alanine dicyclohexylammonium salt emerges as a cornerstone in the rational design of drug candidates boasting enhanced therapeutic potential. Its unique structural profile holds the promise of instilling desirable pharmacological attributes such as heightened efficacy and improved bioavailability propelling scientists towards unprecedented frontiers in medicinal chemistry and drug optimization.

Protein Engineering: Illuminating the realm of protein engineering the utility of Boc-β-(2-thienyl)-D-alanine dicyclohexylammonium salt shines brightly facilitating the transformation of amino acid sequences to yield proteins endowed with novel functionalities and enhanced properties. The integration of this compound into proteins introduces bespoke chemical characteristics essential for investigating protein interactions and fortifying stability establishing a cornerstone in the advancement of biotechnological innovations and therapeutic protein development.

Enzyme Activity Studies: Employed in enzymology Boc-β-(2-thienyl)-D-alanine dicyclohexylammonium salt serves as a pivotal instrument in unraveling the intricate dynamics of enzyme-substrate interactions and enzymatic catalysis. By incorporating Boc-β-(2-thienyl)-D-alanine derivatives into substrate analogs, researchers unlock a realm of precision in scrutinizing enzyme binding and activity leading to a deeper understanding of enzyme mechanisms. This wealth of knowledge propels the creation of enzyme modulators whether inhibitors or activators paving the way for pioneering therapeutic avenues.

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