Boc-β-(3-thienyl)-L-alanine dicyclohexylammonium salt
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Boc-β-(3-thienyl)-L-alanine dicyclohexylammonium salt

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Category
BOC-Amino Acids
Catalog number
BAT-007931
CAS number
83825-42-7
Molecular Formula
C12H17NO4S·C12H23N
Molecular Weight
452.65
Boc-β-(3-thienyl)-L-alanine dicyclohexylammonium salt
IUPAC Name
N-cyclohexylcyclohexanamine;(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-thiophen-3-ylpropanoic acid
Synonyms
Boc-3-L-Ala(3-thienyl)-OH DCHA; Boc-L-3-Thienylalanine-DCHA; dicyclohexylamine (S)-2-((tert-butoxycarbonyl)amino)-3-(thiophen-3-yl)propanoate; Boc-beta-(3-thienyl)-D-Ala-OH DCHA; N-cyclohexylcyclohexanamine;(2S)-2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-thiophen-3-ylpropanoic acid; N-cyclohexylcyclohexanamine; 2-[(2-methylpropan-2-yl)oxycarbonylamino]-3-thiophen-3-yl-propanoic acid; N-cyclohexylcyclohexanamine
Related CAS
109007-59-2 (free base)
Appearance
White to pale yellow powder
Purity
≥ 98% (HPLC)
Density
1.243g/cm3
Boiling Point
434.7°C at 760 mmHg
Storage
Store at 2-8 °C
InChI
InChI=1S/C12H17NO4S.C12H23N/c1-12(2,3)17-11(16)13-9(10(14)15)6-8-4-5-18-7-8;1-3-7-11(8-4-1)13-12-9-5-2-6-10-12/h4-5,7,9H,6H2,1-3H3,(H,13,16)(H,14,15);11-13H,1-10H2/t9-;/m0./s1
InChI Key
FNTVEJPWKBETJW-FVGYRXGTSA-N
Canonical SMILES
CC(C)(C)OC(=O)NC(CC1=CSC=C1)C(=O)O.C1CCC(CC1)NC2CCCCC2

Boc-β-(3-thienyl)-L-alanine dicyclohexylammonium salt is a chemical compound used in various research and development applications. Here are some key applications of Boc-β-(3-thienyl)-L-alanine dicyclohexylammonium salt:

Peptide Synthesis: Boc-β-(3-thienyl)-L-alanine dicyclohexylammonium salt is commonly employed in the synthesis of peptides due to its role as a protected amino acid. It allows for the sequential addition of amino acids without premature reactions ensuring correct peptide sequences. This is crucial for creating biologically active peptides for research and therapeutic use.

Drug Development: In pharmaceutical research, Boc-β-(3-thienyl)-L-alanine dicyclohexylammonium salt is used to develop peptide-based drug candidates. Its incorporation into peptide chains can enhance the drug's stability and bioavailability. Researchers use this compound to design and optimize new therapeutics targeting various diseases.

Structural Biology: Boc-β-(3-thienyl)-L-alanine dicyclohexylammonium salt can be used in structural biology studies to understand protein folding and interactions. By incorporating this compound into peptides and proteins, scientists can explore how specific amino acid modifications affect structure and function. This is valuable for elucidating mechanisms of protein behavior and function.

Chemical Biology: This compound serves as a tool in chemical biology for studying the interactions between peptides and other biological molecules. Its unique thienyl group can provide insights into hydrophobic interactions and binding affinities. Researchers utilize it to probe biochemical pathways and identify key molecular interactions regulating biological processes.

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