(1S,2S)-2-((R)-1-Phenylethylamino)Cyclohexanol

96%

Reagent Code: #237367
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CAS Number 98361-56-9

science Other reagents with same CAS 98361-56-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 219.32 g/mol
Formula C₁₄H₂₁NO
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Widely used as a chiral auxiliary and resolving agent in asymmetric synthesis, this compound plays a key role in the preparation of enantiomerically pure amines and alcohols. Its rigid cyclohexanol backbone and well-defined stereochemistry make it ideal for inducing chirality in catalytic reactions, particularly in enantioselective reductions and aminations. It is also employed in the pharmaceutical industry for the resolution of racemic mixtures, enabling the isolation of single-enantiomer intermediates critical to drug development. Due to its ability to form stable diastereomeric complexes, it is frequently applied in chiral separations and purification processes. Additionally, it serves as a building block in the synthesis of bioactive molecules and natural products where stereocontrol is essential.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,840.00
(1S,2S)-2-((R)-1-Phenylethylamino)Cyclohexanol
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Widely used as a chiral auxiliary and resolving agent in asymmetric synthesis, this compound plays a key role in the preparation of enantiomerically pure amines and alcohols. Its rigid cyclohexanol backbone and well-defined stereochemistry make it ideal for inducing chirality in catalytic reactions, particularly in enantioselective reductions and aminations. It is also employed in the pharmaceutical industry for the resolution of racemic mixtures, enabling the isolation of single-enantiomer intermediates

Widely used as a chiral auxiliary and resolving agent in asymmetric synthesis, this compound plays a key role in the preparation of enantiomerically pure amines and alcohols. Its rigid cyclohexanol backbone and well-defined stereochemistry make it ideal for inducing chirality in catalytic reactions, particularly in enantioselective reductions and aminations. It is also employed in the pharmaceutical industry for the resolution of racemic mixtures, enabling the isolation of single-enantiomer intermediates critical to drug development. Due to its ability to form stable diastereomeric complexes, it is frequently applied in chiral separations and purification processes. Additionally, it serves as a building block in the synthesis of bioactive molecules and natural products where stereocontrol is essential.

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