(R)-1-N-Boc-3-Methanesulfonyloxypiperidine

98%

Reagent Code: #230451
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CAS Number 404577-34-0

science Other reagents with same CAS 404577-34-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 279.35 g/mol
Formula C₁₁H₂₁NO₅S
badge Registry Numbers
MDL Number MFCD09953026
thermostat Physical Properties
Boiling Point 407.2°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry seal

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of bioactive molecules with central nervous system activity. Its protected amine and activated sulfonate ester functionalities allow selective nucleophilic substitution, enabling efficient construction of complex piperidine-containing structures. Commonly employed in medicinal chemistry for the preparation of protease inhibitors, receptor agonists, and antagonists. The Boc-protected group ensures stability during multi-step syntheses, while the mesylate group serves as a good leaving group for displacement reactions. Widely utilized in asymmetric synthesis to maintain stereochemical integrity in final drug candidates.

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Test Parameter Specification
Appearance White to Off-White Solid
Purity (%) 97.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿3,670.00
inventory 5g
10-20 days ฿14,730.00
inventory 10g
10-20 days ฿25,650.00

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(R)-1-N-Boc-3-Methanesulfonyloxypiperidine
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Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of bioactive molecules with central nervous system activity. Its protected amine and activated sulfonate ester functionalities allow selective nucleophilic substitution, enabling efficient construction of complex piperidine-containing structures. Commonly employed in medicinal chemistry for the preparation of protease inhibitors, receptor agonists, and antagonists. The Boc-protected group ensures stability during multi-step syntheses, while the mesylate group serves as a good leaving group for displacement reactions. Widely utilized in asymmetric synthesis to maintain stereochemical integrity in final drug candidates.
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