cis-1-Boc-4-aminomethyl-3-hydroxypiperidine
97%
Reagent
Code: #123378
CAS Number
219985-15-6
blur_circular Chemical Specifications
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Molecular Information
Weight
230.3 g/mol
Formula
C₁₁H₂₂N₂O₃
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Registry Numbers
MDL Number
MFCD18791264
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Storage & Handling
Storage
2-8°C, protected from light
description Product Description
This compound is primarily utilized in the synthesis of pharmaceutical intermediates, particularly in the development of active pharmaceutical ingredients (APIs). Its structure, featuring a Boc-protected piperidine nitrogen, a primary aminomethyl group at position 4, and a hydroxyl group at position 3 in a cis configuration, makes it a versatile building block in organic synthesis. It is often employed in the creation of complex molecules, including those used in the treatment of neurological disorders and other therapeutic areas. The Boc group provides protection for the piperidine nitrogen during synthetic processes, allowing for selective reactions at other sites, while the unprotected aminomethyl offers an additional reactive amine functionality. The hydroxyl group can be further modified or used as a handle for coupling reactions, enhancing its utility in medicinal chemistry. Its application is particularly significant in the design of piperidine-based compounds, which are common in drug discovery due to their biological activity.
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