3-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)pyridine

95%

Reagent Code: #89978
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CAS Number 1362703-30-7

science Other reagents with same CAS 1362703-30-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 297.16 g/mol
Formula C₁₇H₂₀BNO₃
badge Registry Numbers
MDL Number MFCD28390310
inventory_2 Storage & Handling
Storage Room temperature, sealed, dry

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group enables the formation of carbon-carbon bonds, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. It is also employed in the synthesis of complex organic molecules, including bioactive compounds and polymers, due to its stability and reactivity under mild conditions. Additionally, it serves as a key intermediate in the preparation of boron-containing compounds, which are increasingly important in medicinal chemistry and material science.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,285.00
inventory 250mg
10-20 days ฿22,815.00

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3-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)pyridine
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This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group enables the formation of carbon-carbon bonds, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. It is also employed in the synthesis of complex organic molecules, including bioactive compounds and polymers, due to its stability and reactivity under mild conditions. Additionally, it serves as a key in

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group enables the formation of carbon-carbon bonds, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. It is also employed in the synthesis of complex organic molecules, including bioactive compounds and polymers, due to its stability and reactivity under mild conditions. Additionally, it serves as a key intermediate in the preparation of boron-containing compounds, which are increasingly important in medicinal chemistry and material science.

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