L-Cyclohexylalaninol hydrochloride
Need Assistance?
  • US & Canada:
    +
  • UK: +

L-Cyclohexylalaninol hydrochloride

* Please kindly note that our products are not to be used for therapeutic purposes and cannot be sold to patients.

Category
Amino Alcohol
Catalog number
BAT-002638
CAS number
117160-99-3
Molecular Formula
C9H20ClNO
Molecular Weight
193.72
L-Cyclohexylalaninol hydrochloride
IUPAC Name
(2S)-2-amino-3-cyclohexylpropan-1-ol;hydrochloride
Synonyms
H-Cha-ol HCl; H-Phe(hexahydro)-ol HCl; (S)-2-Amino-3-cyclohexyl-1-propanol hydrochloride; (S)-(+)-2-Amino-3-cyclohexyl-1-propanol hydrochloride; (2S)-2-amino-3-cyclohexylpropan-1-ol hydrochloride
Purity
≥ 95%
Density
0.970 g/cm3
Melting Point
230 °C (dec.)(lit.)
Boiling Point
289.5 °C at 760 mmHg
InChI
InChI=1S/C9H19NO.ClH/c10-9(7-11)6-8-4-2-1-3-5-8;/h8-9,11H,1-7,10H2;1H/t9-;/m0./s1
InChI Key
BMHYDTXNZNVADC-FVGYRXGTSA-N
Canonical SMILES
C1CCC(CC1)CC(CO)N.Cl

L-Cyclohexylalaninol hydrochloride, a specialized compound with diverse applications in medicinal chemistry and drug development, plays a pivotal role in various fields. Here are the key applications of L-Cyclohexylalaninol hydrochloride presented with high perplexity and burstiness:

Peptidomimetics Synthesis: Engage in the art of peptidomimetics synthesis with L-Cyclohexylalaninol hydrochloride, a compound that weaves complexity and functionality into the mimicry of peptides' structures and actions. By creating stable analogs that defy enzymatic degradation, this compound becomes indispensable in crafting therapeutic agents targeting peptide pathways in diseases.

Chiral Building Block: Behold the significance of L-Cyclohexylalaninol hydrochloride as a critical chiral building block in the grand orchestration of organic synthesis. With its stereochemical prowess, this compound bestows upon chemists the power to construct intricate molecules with precise chirality. The resulting three-dimensional structures are vital in formulating pharmaceuticals that interact harmoniously with biological targets.

Research in Protein-Protein Interactions: Delve into the realm of protein-protein interactions with L-Cyclohexylalaninol hydrochloride as your guide. As researchers embed this compound into synthetic peptides or drugs, they unlock the secrets of how interactions between proteins influence cellular processes. This newfound knowledge serves as a beacon illuminating new drug targets and unraveling the intricate mechanisms of disease.

Development of New Therapeutics: Witness the transformative journey of drug discovery fueled by L-Cyclohexylalaninol hydrochloride, a catalyst for the inception of novel therapeutic agents. Through its unique chemical properties, this compound acts as a versatile scaffold for attaching diverse functional groups birthing groundbreaking drugs with enhanced efficacy and safety profiles. This innovative approach expedites the quest for new treatments across a spectrum of diseases ushering in a new era of healing and hope.

1. 1-Haloacylpiperazines
S Groszkowski, J Sienkiewicz, L Korzycka Pol J Pharmacol Pharm. 1975 Apr-Jun;27(2):183-6.
By direct acylation of piperazine with halogenocarboxylic acid chlorides in acid medium, the hydrochlorides of 1-haloacylpiperazines were obtained.
2. Metal-free and regiospecific synthesis of 3-arylindoles
Chuangchuang Xu, Wenlai Xie, Jiaxi Xu Org Biomol Chem. 2020 Apr 8;18(14):2661-2671. doi: 10.1039/d0ob00317d.
A convenient, metal-free, and organic acid-base promoted synthetic method to prepare 3-arylindoles from 3-aryloxirane-2-carbonitriles and arylhydrazine hydrochlorides has been developed. In the reaction, the organic acid catalyzes a tandem nucleophilic ring-opening reaction of aryloxiranecarbonitriles and arylhydrazine hydrochlorides and Fischer indolization. The organic base triethylamine plays a crucial role in the final elimination step in the Fischer indole synthesis, affording 3-arylindoles regiospecifically. The reaction features advantages of microwave acceleration, non-metal participation, short reaction time, organic acid-base co-catalysis, and broad substrate scope.
Online Inquiry
Verification code
Inquiry Basket