1-(2-Methoxy-2-oxoethyl)-6-oxo-1,6-dihydropyridine-3-boronic Acid Pinacol Ester

95%

Reagent Code: #89456

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 293.12 g/mol
Formula C₁₄H₂₀NO₅B
badge Registry Numbers
MDL Number MFCD28133363
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. The boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. Its stability and reactivity make it suitable for synthesizing biologically active compounds, including drug candidates and fine chemicals. Additionally, it is often employed in the development of materials science applications, such as creating advanced polymers or functionalized surfaces.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿13,932.00
inventory 1g
10-20 days ฿37,152.00

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1-(2-Methoxy-2-oxoethyl)-6-oxo-1,6-dihydropyridine-3-boronic Acid Pinacol Ester
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. The boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. Its stability and reactivity make it suitable for synthesizing biologically active compounds, including drug cand

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in the pharmaceutical and agrochemical industries. The boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. Its stability and reactivity make it suitable for synthesizing biologically active compounds, including drug candidates and fine chemicals. Additionally, it is often employed in the development of materials science applications, such as creating advanced polymers or functionalized surfaces.

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