3-Fluoro-4-(2-(4-hydroxypiperidin-1-yl)ethoxy)phenylboronic acid
98%
Reagent
Code: #90146
CAS Number
1704064-11-8
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Molecular Information
Weight
283.11 g/mol
Formula
C₁₃H₁₉BFNO₄
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Registry Numbers
MDL Number
MFCD28400174
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Storage & Handling
Storage
2-8°C
description Product Description
This compound is primarily utilized in organic synthesis and medicinal chemistry due to its boronic acid functional group, which makes it a valuable building block for Suzuki-Miyaura cross-coupling reactions. These reactions are widely employed in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The presence of the hydroxypiperidine moiety enhances its potential as a pharmacophore, making it useful in the development of drug candidates, particularly those targeting neurological or metabolic disorders. Additionally, its fluorine atom can improve metabolic stability and bioavailability, making it a promising intermediate in the design of bioactive molecules.
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3-Fluoro-4-(2-(4-hydroxypiperidin-1-yl)ethoxy)phenylboronic acid
This compound is primarily utilized in organic synthesis and medicinal chemistry due to its boronic acid functional group, which makes it a valuable building block for Suzuki-Miyaura cross-coupling reactions. These reactions are widely employed in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The presence of the hydroxypiperidine moiety enhances its potential as a pharmacophore, making it useful in the development of drug candidates, particularly those targeting neurological or metabolic disorders. Additionally, its fluorine atom can improve metabolic stability and bioavailability, making it a promising intermediate in the design of bioactive molecules.
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