S-1-Boc-3-hydroxypiperidine

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Reagent Code: #234230
label
Alias (S)-1-tert-butoxycarbonyl-3-hydroxypiperidine (S)-1-Boc-3-hydroxypiperidine
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CAS Number 143900-44-1

science Other reagents with same CAS 143900-44-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.27 g/mol
Formula C₁₀H₁₉NO₃
badge Registry Numbers
MDL Number MFCD04115307
thermostat Physical Properties
Melting Point 34-40 °C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring chiral piperidine scaffolds. Its protected hydroxyl and amine functionalities allow selective reactions in multi-step organic syntheses. Commonly employed in the production of central nervous system (CNS) agents, including antidepressants and antipsychotics. Also utilized in the preparation of protease inhibitors and other bioactive molecules where a functionalized piperidine ring is required. The Boc-protected amine ensures stability during reactions and enables deprotection under mild acidic conditions, making it suitable for complex molecule assembly.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿174.00
inventory 5g
10-20 days ฿310.00
inventory 25g
10-20 days ฿880.00
inventory 100g
10-20 days ฿3,490.00
inventory 500g
10-20 days ฿15,000.00

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S-1-Boc-3-hydroxypiperidine
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring chiral piperidine scaffolds. Its protected hydroxyl and amine functionalities allow selective reactions in multi-step organic syntheses. Commonly employed in the production of central nervous system (CNS) agents, including antidepressants and antipsychotics. Also utilized in the preparation of protease inhibitors and other bioactive molecules where a functi

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring chiral piperidine scaffolds. Its protected hydroxyl and amine functionalities allow selective reactions in multi-step organic syntheses. Commonly employed in the production of central nervous system (CNS) agents, including antidepressants and antipsychotics. Also utilized in the preparation of protease inhibitors and other bioactive molecules where a functionalized piperidine ring is required. The Boc-protected amine ensures stability during reactions and enables deprotection under mild acidic conditions, making it suitable for complex molecule assembly.

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