rel-Benzyl (3R,4R)-3-((tert-butoxycarbonyl)amino)-4-hydroxypiperidine-1-carboxylate

98%

Reagent Code: #124565
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CAS Number 859854-67-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 350.41 g/mol
Formula C₁₈H₂₆N₂O₅
badge Registry Numbers
MDL Number MFCD13152269
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the development of biologically active compounds, including potential drug candidates. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and a piperidine ring, makes it valuable for constructing peptides and other nitrogen-containing heterocycles. The Boc group can be selectively removed under mild acidic conditions, allowing for further functionalization. Additionally, the hydroxyl and amino groups provide sites for chemical modifications, enabling the creation of diverse derivatives for medicinal chemistry applications. Its role in the production of protease inhibitors and other therapeutic agents highlights its importance in drug discovery and development.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿28,107.00
inventory 100mg
10-20 days ฿7,668.00
inventory 250mg
10-20 days ฿14,049.00
rel-Benzyl (3R,4R)-3-((tert-butoxycarbonyl)amino)-4-hydroxypiperidine-1-carboxylate
This compound is primarily utilized in the synthesis of complex organic molecules, particularly in pharmaceutical research. It serves as a key intermediate in the development of biologically active compounds, including potential drug candidates. Its structure, featuring both a tert-butoxycarbonyl (Boc) protecting group and a piperidine ring, makes it valuable for constructing peptides and other nitrogen-containing heterocycles. The Boc group can be selectively removed under mild acidic conditions, allowing for further functionalization. Additionally, the hydroxyl and amino groups provide sites for chemical modifications, enabling the creation of diverse derivatives for medicinal chemistry applications. Its role in the production of protease inhibitors and other therapeutic agents highlights its importance in drug discovery and development.
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