(3-Fluoro-4-(2-(4-methylpiperidin-1-yl)ethoxy) phenyl)boronic acid hydrochloride

98%

Reagent Code: #89109
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CAS Number 1704095-74-8

science Other reagents with same CAS 1704095-74-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 317.59 g/mol
Formula C₁₄H₂₂BClFNO₃
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This compound is primarily utilized in organic synthesis and pharmaceutical research due to its boronic acid functional group, which is instrumental in Suzuki-Miyaura cross-coupling reactions. These reactions are pivotal for forming carbon-carbon bonds, enabling the synthesis of complex organic molecules, including potential drug candidates. The presence of the fluorine atom enhances the compound's reactivity and selectivity in these reactions, making it valuable for creating biologically active molecules. Additionally, the piperidine moiety contributes to the compound's ability to interact with biological targets, particularly in the development of central nervous system (CNS) drugs. Its hydrochloride form ensures improved solubility and stability, facilitating its use in various experimental and industrial processes.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿38,520.00
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(3-Fluoro-4-(2-(4-methylpiperidin-1-yl)ethoxy) phenyl)boronic acid hydrochloride
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This compound is primarily utilized in organic synthesis and pharmaceutical research due to its boronic acid functional group, which is instrumental in Suzuki-Miyaura cross-coupling reactions. These reactions are pivotal for forming carbon-carbon bonds, enabling the synthesis of complex organic molecules, including potential drug candidates. The presence of the fluorine atom enhances the compound's reactivity and selectivity in these reactions, making it valuable for creating biologically active molecule

This compound is primarily utilized in organic synthesis and pharmaceutical research due to its boronic acid functional group, which is instrumental in Suzuki-Miyaura cross-coupling reactions. These reactions are pivotal for forming carbon-carbon bonds, enabling the synthesis of complex organic molecules, including potential drug candidates. The presence of the fluorine atom enhances the compound's reactivity and selectivity in these reactions, making it valuable for creating biologically active molecules. Additionally, the piperidine moiety contributes to the compound's ability to interact with biological targets, particularly in the development of central nervous system (CNS) drugs. Its hydrochloride form ensures improved solubility and stability, facilitating its use in various experimental and industrial processes.

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