2-Methyl-6-(piperidin-4-yl)pyridine-4-boronic acid

95%

Reagent Code: #91761
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CAS Number 2225171-83-3

science Other reagents with same CAS 2225171-83-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 220.07588 g/mol
Formula C₁₁H₁₇BN₂O₂
inventory_2 Storage & Handling
Storage -20℃, sealed and dry

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions, where it acts as a key building block for the formation of carbon-carbon bonds. Its boronic acid group enables it to participate in Suzuki-Miyaura reactions, which are widely employed in the pharmaceutical industry for the synthesis of complex molecules, including drug candidates. Additionally, it serves as an intermediate in the development of biologically active compounds, such as enzyme inhibitors or receptor modulators, due to its structural versatility. The piperidine moiety further enhances its potential in drug discovery, as it is a common pharmacophore in medicinal chemistry. Its applications also extend to materials science, where it can be used to create functionalized polymers or advanced materials with specific properties.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿86,080.00
inventory 25mg
10-20 days ฿223,800.00

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2-Methyl-6-(piperidin-4-yl)pyridine-4-boronic acid
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions, where it acts as a key building block for the formation of carbon-carbon bonds. Its boronic acid group enables it to participate in Suzuki-Miyaura reactions, which are widely employed in the pharmaceutical industry for the synthesis of complex molecules, including drug candidates. Additionally, it serves as an intermediate in the development of biologically active compounds, such as enzyme inhibitors or re

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions, where it acts as a key building block for the formation of carbon-carbon bonds. Its boronic acid group enables it to participate in Suzuki-Miyaura reactions, which are widely employed in the pharmaceutical industry for the synthesis of complex molecules, including drug candidates. Additionally, it serves as an intermediate in the development of biologically active compounds, such as enzyme inhibitors or receptor modulators, due to its structural versatility. The piperidine moiety further enhances its potential in drug discovery, as it is a common pharmacophore in medicinal chemistry. Its applications also extend to materials science, where it can be used to create functionalized polymers or advanced materials with specific properties.

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