(R)-tert-Butyl 5-hydroxy-3,3-dimethylpiperidine-1-carboxylate

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Reagent Code: #228647
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CAS Number 1189570-45-3

science Other reagents with same CAS 1189570-45-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 229.32 g/mol
Formula C₁₂H₂₃NO₃
badge Registry Numbers
MDL Number MFCD30471616
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents. This (R)-configured compound features a piperidine core with a hydroxyl group at position 5, geminal dimethyl groups at position 3, and an N-tert-butoxycarbonyl (Boc) protecting group. These structural elements enable precise modifications for optimizing pharmacokinetic properties and control in synthetic reactions. The compound is valuable in asymmetric synthesis due to its stereochemical purity, making it suitable for creating enantiomerically pure drugs. Commonly employed in the preparation of bioactive molecules where the (R)-configuration is critical for activity.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿46,000.00
(R)-tert-Butyl 5-hydroxy-3,3-dimethylpiperidine-1-carboxylate
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents. This (R)-configured compound features a piperidine core with a hydroxyl group at position 5, geminal dimethyl groups at position 3, and an N-tert-butoxycarbonyl (Boc) protecting group. These structural elements enable precise modifications for optimizing pharmacokinetic properties and control in synthetic reactions. The compound is valuable in asymmetric synthesis d

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) agents. This (R)-configured compound features a piperidine core with a hydroxyl group at position 5, geminal dimethyl groups at position 3, and an N-tert-butoxycarbonyl (Boc) protecting group. These structural elements enable precise modifications for optimizing pharmacokinetic properties and control in synthetic reactions. The compound is valuable in asymmetric synthesis due to its stereochemical purity, making it suitable for creating enantiomerically pure drugs. Commonly employed in the preparation of bioactive molecules where the (R)-configuration is critical for activity.

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