1-Boc-3-hydroxypiperidine

98%

Reagent Code: #143461
label
Alias tert-butyl 3-hydroxy-1-piperidinic acid
fingerprint
CAS Number 85275-45-2

science Other reagents with same CAS 85275-45-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.26 g/mol
Formula C₁₀H₁₉NO₃
badge Registry Numbers
MDL Number MFCD02093938
thermostat Physical Properties
Melting Point 65-67°C
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) where piperidine derivatives are required. Its hydroxyl and Boc-protected amine functionalities allow selective reactions, making it valuable in constructing complex molecules. Commonly employed in medicinal chemistry for drug discovery, especially in central nervous system agents, kinase inhibitors, and receptor modulators. The compound’s structure supports conformational control, enhancing drug potency and selectivity. Also utilized in solid-phase synthesis and combinatorial chemistry due to its stability and ease of deprotection.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿137.50
5g
10-20 days ฿154.00
25g
10-20 days ฿340.00
100g
10-20 days ฿1,270.00
500g
10-20 days ฿4,750.00
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) where piperidine derivatives are required. Its hydroxyl and Boc-protected amine functionalities allow selective reactions, making it valuable in constructing complex molecules. Commonly employed in medicinal chemistry for drug discovery, especially in central nervous system agents, kinase inhibitors, and receptor modulators. The compound’s structure supports conformational control, enhancing drug potency and selectivity. Also utilized in solid-phase synthesis and combinatorial chemistry due to its stability and ease of deprotection.
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