tert-butyl 4-nitropiperidine-1-carboxylate

97%

Reagent Code: #242508
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CAS Number 1228630-89-4

science Other reagents with same CAS 1228630-89-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.26 g/mol
Formula C₁₀H₁₈N₂O₄
thermostat Physical Properties
Boiling Point 327.7±31.0℃(Predicted)
inventory_2 Storage & Handling
Density 1.16±0.1 g/cm3(Predicted)
Storage 2-8℃

description Product Description

Used as an intermediate in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) where the piperidine ring serves as a structural backbone. The nitro group allows for further functionalization, such as reduction to an amine, enabling the formation of nitrogen-containing compounds important in drug design. The tert-butyloxycarbonyl (Boc) protecting group ensures selective reactivity during multi-step syntheses, making this compound valuable in the preparation of complex molecules, including those with central nervous system activity. Commonly employed in research settings for the synthesis of piperidine-based derivatives with potential therapeutic effects.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,160.00
inventory 1g
10-20 days ฿2,790.00

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tert-butyl 4-nitropiperidine-1-carboxylate
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Used as an intermediate in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) where the piperidine ring serves as a structural backbone. The nitro group allows for further functionalization, such as reduction to an amine, enabling the formation of nitrogen-containing compounds important in drug design. The tert-butyloxycarbonyl (Boc) protecting group ensures selective reactivity during multi-step syntheses, making this compound valuable in the preparatio

Used as an intermediate in pharmaceutical synthesis, particularly in the development of active pharmaceutical ingredients (APIs) where the piperidine ring serves as a structural backbone. The nitro group allows for further functionalization, such as reduction to an amine, enabling the formation of nitrogen-containing compounds important in drug design. The tert-butyloxycarbonyl (Boc) protecting group ensures selective reactivity during multi-step syntheses, making this compound valuable in the preparation of complex molecules, including those with central nervous system activity. Commonly employed in research settings for the synthesis of piperidine-based derivatives with potential therapeutic effects.

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