Tert-butyl 3-nitropiperidine-1-carboxylate

98%

Reagent Code: #239024
label
Alias 3-Nitropiperidine-1-carboxylate tert-butyl ester
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CAS Number 1313738-96-3

science Other reagents with same CAS 1313738-96-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.26 g/mol
Formula C₁₀H₁₈N₂O₄
badge Registry Numbers
MDL Number MFCD19443921
thermostat Physical Properties
Boiling Point 327.7±31.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.16±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

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 more complex molecules. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactivity during multi-step syntheses, making it valuable in the preparation of nitrogen-containing heterocyclic compounds for medicinal chemistry research. Commonly employed in the synthesis of central nervous system (CNS) agents, including potential antidepressants, antipsychotics, and cognitive enhancers.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿8,220.00
inventory 250mg
10-20 days ฿15,660.00

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Tert-butyl 3-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 more complex molecules. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactivity during multi-step syntheses, making it valuable in the preparation of nitrogen-containing heterocyclic compoun

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 more complex molecules. The tert-butoxycarbonyl (Boc) protecting group ensures selective reactivity during multi-step syntheses, making it valuable in the preparation of nitrogen-containing heterocyclic compounds for medicinal chemistry research. Commonly employed in the synthesis of central nervous system (CNS) agents, including potential antidepressants, antipsychotics, and cognitive enhancers.

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