benzyl 4-((tert-butoxycarbonyl)amino)-4-methylpiperidine-1-carboxylate

95%

Reagent Code: #83763
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CAS Number 169750-60-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 348.44 g/mol
Formula C₁₉H₂₈N₂O₄
badge Registry Numbers
MDL Number MFCD23099450
thermostat Physical Properties
Boiling Point 473.1±44.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.14±0.1 g/cm3(Predicted)
Storage room temperature

description Product Description

This compound is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceuticals. It serves as a key intermediate in the synthesis of complex molecules, especially those involving piperidine derivatives. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and a benzyl ester, makes it valuable in peptide and medicinal chemistry. The Boc group is commonly used to protect amines during multi-step synthetic processes, while the benzyl ester can be selectively removed under mild conditions. This chemical is often employed in the preparation of biologically active compounds, including potential drug candidates targeting neurological disorders, due to the piperidine moiety’s presence in many pharmacologically relevant structures. Its application extends to the synthesis of inhibitors, receptor modulators, and other therapeutic agents.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days €139.01
inventory 1g
10-20 days €278.01
inventory 5g
10-20 days €834.04
benzyl 4-((tert-butoxycarbonyl)amino)-4-methylpiperidine-1-carboxylate
This compound is primarily utilized in the field of organic synthesis, particularly in the development of pharmaceuticals. It serves as a key intermediate in the synthesis of complex molecules, especially those involving piperidine derivatives. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and a benzyl ester, makes it valuable in peptide and medicinal chemistry. The Boc group is commonly used to protect amines during multi-step synthetic processes, while the benzyl ester can be selectively removed under mild conditions. This chemical is often employed in the preparation of biologically active compounds, including potential drug candidates targeting neurological disorders, due to the piperidine moiety’s presence in many pharmacologically relevant structures. Its application extends to the synthesis of inhibitors, receptor modulators, and other therapeutic agents.
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