N-Carbobenzoxy-L-cyclohexylalaninol
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N-Carbobenzoxy-L-cyclohexylalaninol

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Category
Amino Alcohol
Catalog number
BAT-002667
CAS number
113828-85-6
Molecular Formula
C17H25NO3
Molecular Weight
291.38
N-Carbobenzoxy-L-cyclohexylalaninol
IUPAC Name
benzyl N-[(2S)-1-cyclohexyl-3-hydroxypropan-2-yl]carbamate
Synonyms
Z-Cha-ol; Z-Phe(hexahydro)-ol; (S)-2-(Carbobenzoxyamino)-3-cyclohexyl-1-propanol; N-CARBOBENZOXY-L-CYCLOHEXYLALANINOL; (S)-benzyl 1-cyclohexyl-3-hydroxypropan-2-ylcarbamate; N-[(1S)-2-Cyclohexyl-1-(hydroxymethyl)ethyl]carbamic acid benzyl ester
Purity
95%
InChI
InChI=1S/C17H23NO4/c19-16(20)15(11-13-7-3-1-4-8-13)18-17(21)22-12-14-9-5-2-6-10-14/h2,5-6,9-10,13,15H,1,3-4,7-8,11-12H2,(H,18,21)(H,19,20)/t15-/m1/s1
InChI Key
MNABZONTQXNLDT-OAHLLOKOSA-N
Canonical SMILES
C1CCC(CC1)CC(C(=O)O)NC(=O)OCC2=CC=CC=C2

N-Carbobenzoxy-L-cyclohexylalaninol, a compound frequently utilized in peptide synthesis and pharmaceutical research, has diverse applications. Here are the key applications portrayed with elevated perplexity and burstiness:

Peptide Synthesis: Serving as a foundational element in the creation of intricate peptides, N-Carbobenzoxy-L-cyclohexylalaninol plays a crucial role. It shields the amino group throughout peptide chain assembly safeguarding against undesired side reactions. This meticulous protection is essential for generating high-purity peptides vital for both research endeavors and therapeutic applications.

Pharmaceutical Research: Positioned at the forefront of pharmaceutical exploration, this compound acts as a progenitor for novel pharmacologically active compounds. Researchers harness its potential to craft analogues and derivatives that may showcase enhanced therapeutic attributes. These investigations aid in pinpointing potential drug candidates catering to a diverse array of medical conditions.

Enzyme Inhibition Studies: Within the realm of enzyme-substrate interactions, N-Carbobenzoxy-L-cyclohexylalaninol assumes a key role as a competitive inhibitor illuminating crucial insights into enzyme mechanics. By discerning its inhibitory effects on specific enzymes, researchers unveil potential intervention points for drug development steering the design of more potent enzyme-targeted therapies.

Chemical Synthesis Optimization: In the intricate landscape of chemical synthesis, N-Carbobenzoxy-L-cyclohexylalaninol emerges as a valuable asset for refining reaction conditions and enhancing yields. Its utility extends to optimizing protection and deprotection strategies within complex synthetic pathways. Ensuring utmost efficiency in these processes is indispensable for facilitating scalable and cost-effective chemical production

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