N-Boc-3-Mesyloxypiperidine

98%

Reagent Code: #217537
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CAS Number 129888-60-4

science Other reagents with same CAS 129888-60-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 279.35 g/mol
Formula C₁₁H₂₁NO₅S
inventory_2 Storage & Handling
Storage Room temperature, dry

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) where protection of the amine group is required. The Boc (tert-butoxycarbonyl) group provides reversible amine protection during multi-step syntheses, while the mesylate (methanesulfonate) group acts as a good leaving group, enabling nucleophilic substitution reactions. Commonly employed in the preparation of piperidine-based drug candidates, including those targeting central nervous system disorders and other therapeutic areas requiring nitrogen-containing heterocycles. Its structure allows for selective functionalization at specific positions, making it valuable in medicinal chemistry for building complex molecules with high purity and yield.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿280.00
inventory 5g
10-20 days ฿2,090.00
inventory 1g
10-20 days ฿680.00
N-Boc-3-Mesyloxypiperidine
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) where protection of the amine group is required. The Boc (tert-butoxycarbonyl) group provides reversible amine protection during multi-step syntheses, while the mesylate (methanesulfonate) group acts as a good leaving group, enabling nucleophilic substitution reactions. Commonly employed in the preparation of piperidine-based drug candidates, including those ta

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs) where protection of the amine group is required. The Boc (tert-butoxycarbonyl) group provides reversible amine protection during multi-step syntheses, while the mesylate (methanesulfonate) group acts as a good leaving group, enabling nucleophilic substitution reactions. Commonly employed in the preparation of piperidine-based drug candidates, including those targeting central nervous system disorders and other therapeutic areas requiring nitrogen-containing heterocycles. Its structure allows for selective functionalization at specific positions, making it valuable in medicinal chemistry for building complex molecules with high purity and yield.

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