2-(Piperazin-1-yl)pyridine-4-boronic acid, pinacol ester

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Reagent Code: #41215
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CAS Number 957198-31-1

science Other reagents with same CAS 957198-31-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 289.18 g/mol
Formula C₁₅H₂₄BN₃O₂
badge Registry Numbers
MDL Number MFCD06795687
thermostat Physical Properties
Melting Point 112-116°C
Boiling Point 458.5±40.0℃(Predicted)
inventory_2 Storage & Handling
Density 1.11±0.1 g/cm3(Predicted)
Storage room temperature

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, where it acts as a boronic ester reagent. Its structure allows it to facilitate the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The piperazine moiety enhances its solubility and reactivity, enabling efficient coupling with aryl or vinyl halides. Additionally, it is employed in the development of biologically active compounds, where its boronic acid group plays a crucial role in targeting specific molecular interactions. Its stability and versatility make it a preferred choice in medicinal chemistry and material science research.

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inventory 1g
10-20 days ฿9,558.00

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2-(Piperazin-1-yl)pyridine-4-boronic acid, pinacol ester
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling, where it acts as a boronic ester reagent. Its structure allows it to facilitate the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The piperazine moiety enhances its solubility and reactivity, enabling efficient coupling with aryl or vinyl halides. Additionally, it is employed in the development of biologically active compounds, where its boronic acid group plays a crucial role in targeting specific molecular interactions. Its stability and versatility make it a preferred choice in medicinal chemistry and material science research.
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