3-Fluoro-4-((4-hydroxypiperidin-1-yl)methyl)phenylboronic acid

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Reagent Code: #90143
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CAS Number 1704063-99-9

science Other reagents with same CAS 1704063-99-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 253.08 g/mol
Formula C₁₂H₁₇BFNO₃
badge Registry Numbers
MDL Number MFCD28400167
inventory_2 Storage & Handling
Storage  2-8°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The presence of the hydroxypiperidine moiety enhances its solubility and stability in various reaction conditions, facilitating its use in aqueous or polar solvent systems. Additionally, its fluorine atom can influence the electronic properties of the resulting compounds, potentially improving their biological activity or metabolic stability. This chemical is often employed in the development of drug candidates, where precise structural modifications are crucial for optimizing efficacy and safety.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿29,860.00
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3-Fluoro-4-((4-hydroxypiperidin-1-yl)methyl)phenylboronic acid
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The presence of the hydroxypiperidine moiety enhances its solubility and stability in various reaction conditions, facilitating its use in aqueous or polar solvent systems. Additionally, its fluorine atom can influ

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The presence of the hydroxypiperidine moiety enhances its solubility and stability in various reaction conditions, facilitating its use in aqueous or polar solvent systems. Additionally, its fluorine atom can influence the electronic properties of the resulting compounds, potentially improving their biological activity or metabolic stability. This chemical is often employed in the development of drug candidates, where precise structural modifications are crucial for optimizing efficacy and safety.

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