[3-(piperidine-1-carbonyl)phenyl]boronic acid

98%

Reagent Code: #226423
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CAS Number 850568-34-2

science Other reagents with same CAS 850568-34-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.0713 g/mol
Formula C₁₂H₁₆BNO₃
badge Registry Numbers
MDL Number MFCD04115686
thermostat Physical Properties
Melting Point 150-154 °C
Boiling Point 469.8 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.22 g/cm3
Storage 2-8°C, inert atmosphere

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its boronic acid functional group enables Suzuki-Miyaura cross-coupling reactions, making it valuable in constructing biaryl structures found in bioactive molecules. Commonly employed in medicinal chemistry for lead optimization due to its stability and reactivity profile. Also utilized in the preparation of proteolysis-targeting chimeras (PROTACs) and other targeted therapies where precise molecular design is critical.

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inventory 1g
10-20 days ฿3,410.00

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[3-(piperidine-1-carbonyl)phenyl]boronic acid
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its boronic acid functional group enables Suzuki-Miyaura cross-coupling reactions, making it valuable in constructing biaryl structures found in bioactive molecules. Commonly employed in medicinal chemistry for lead optimization due to its stability and reactivity profile. Also utilized in the preparation of proteolysis-targeting chimeras (PROTACs) and other

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for cancer treatment. Its boronic acid functional group enables Suzuki-Miyaura cross-coupling reactions, making it valuable in constructing biaryl structures found in bioactive molecules. Commonly employed in medicinal chemistry for lead optimization due to its stability and reactivity profile. Also utilized in the preparation of proteolysis-targeting chimeras (PROTACs) and other targeted therapies where precise molecular design is critical.

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