(1R,2S)-2-Aminocyclohexan-1-ol hydrochloride

Name: (1R,2S)-2-Aminocyclohexan-1-ol hydrochloride
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CAS No. 190792-72-4
Cat. No. CS-W008152
Purity≥97%
MDL No.None

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(1R,2S)-2-Aminocyclohexan-1-ol hydrochloride|CS-W008152

Structure of 190792-72-4

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General Information

CAS No. 190792-72-4
Cat. No. CS-W008152
Purity ≥97%
MDL No. None
Storage 4°C, sealed storage, away from moisture
Shipping Room temperature in continental US; may vary elsewhere.
Molecular Formula C₆H₁₄ClNO
Molecular Weight 151.63
Synonym(s) (1R,2S)-2-aminocyclohexanol hydrochloride
SMILES N[C@H]1CCCC[C@H]1O.Cl

Description

This chiral cyclohexanol derivative features a primary amine and hydroxyl group in a trans-1,2 configuration, delivering high stereochemical purity. The hydrochloride salt enhances solubility and stability for use in asymmetric synthesis and medicinal chemistry applications.

Application

(1R,2S)-2-Aminocyclohexan-1-ol hydrochloride serves as a stereochemically defined building block for the synthesis of bioactive molecules and chiral auxiliaries. Its stable, bench-ready form facilitates straightforward handling and purification, while the protected amine and secondary alcohol enable sequential functionalization in multistep syntheses. Widely employed in medicinal chemistry and catalytic asymmetric transformations, it functions as a key scaffold for heterocyclic systems and peptidomimetics requiring defined spatial orientation.

Safety Information

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GHS Pictogram :	GHS No : GHS05
Signal Word : Danger	UN#: 1759
Class : 8	Packing Group : Ⅲ
Hazard Statements : H315-H318
Precautionary Statements : P264-P280-P302+P352-P362

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Computational Chemistry Data

TPSA 46.25
LogP 0.6704
H_Acceptors 2
H_Donors 2
Rotatable_Bonds 0

Other Classifications

Building Blocks Functional Group Alcohol

Building Blocks Skeleton Chiral compounds Chiral Building Blocks

Building Blocks Skeleton Fatty ring compounds Cyclohexane compounds

Key Words

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(1R,2S)-2-Aminocyclohexan-1-ol hydrochloride

CAS No. 190792-72-4

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