(1R,2R)-N-Boc-2-aminocyclohexanol

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Reagent Code: #70794
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CAS Number 155975-19-2

science Other reagents with same CAS 155975-19-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.3 g/mol
Formula C₁₁H₂₁NO₃
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

(1R,2R)-N-Boc-2-aminocyclohexanol is widely used in organic synthesis as a chiral building block for the preparation of pharmaceuticals and fine chemicals. Its stereochemistry makes it valuable in the synthesis of enantiomerically pure compounds, particularly in the development of drugs targeting specific biological pathways. The Boc (tert-butoxycarbonyl) protecting group allows for selective deprotection, enabling further functionalization of the molecule. It is commonly employed in the synthesis of complex natural products, peptidomimetics, and other bioactive molecules. Additionally, it serves as an intermediate in the production of catalysts and ligands for asymmetric catalysis, enhancing the efficiency and selectivity of chemical reactions.

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Test Parameter Specification
Appearance White to off-white solid
Purity 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,160.00
inventory 5g
10-20 days ฿4,880.00
inventory 25g
10-20 days ฿19,900.00

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(1R,2R)-N-Boc-2-aminocyclohexanol
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(1R,2R)-N-Boc-2-aminocyclohexanol is widely used in organic synthesis as a chiral building block for the preparation of pharmaceuticals and fine chemicals. Its stereochemistry makes it valuable in the synthesis of enantiomerically pure compounds, particularly in the development of drugs targeting specific biological pathways. The Boc (tert-butoxycarbonyl) protecting group allows for selective deprotection, enabling further functionalization of the molecule. It is commonly employed in the synthesis of com

(1R,2R)-N-Boc-2-aminocyclohexanol is widely used in organic synthesis as a chiral building block for the preparation of pharmaceuticals and fine chemicals. Its stereochemistry makes it valuable in the synthesis of enantiomerically pure compounds, particularly in the development of drugs targeting specific biological pathways. The Boc (tert-butoxycarbonyl) protecting group allows for selective deprotection, enabling further functionalization of the molecule. It is commonly employed in the synthesis of complex natural products, peptidomimetics, and other bioactive molecules. Additionally, it serves as an intermediate in the production of catalysts and ligands for asymmetric catalysis, enhancing the efficiency and selectivity of chemical reactions.

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