2-[[(tert-Butyldimethylsilyl)oxy]methyl]-6-methylphenylboronic Acid Pinacol Ester

95%

Reagent Code: #89769

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 362.39 g/mol
Formula C₂₀H₃₅O₃BSi
badge Registry Numbers
MDL Number MFCD28101623
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a boronic ester reagent, enabling the formation of carbon-carbon bonds in the presence of a palladium catalyst. Its tert-butyldimethylsilyl (TBDMS) protecting group enhances stability and selectivity during reactions, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The compound is also utilized in the development of advanced materials and fine chemicals, where precise control over molecular structure is essential. Its application is favored in research and industrial settings for its efficiency and reliability in creating diverse chemical architectures.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿18,576.00
inventory 1g
10-20 days ฿43,659.00

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2-[[(tert-Butyldimethylsilyl)oxy]methyl]-6-methylphenylboronic Acid Pinacol Ester
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This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a boronic ester reagent, enabling the formation of carbon-carbon bonds in the presence of a palladium catalyst. Its tert-butyldimethylsilyl (TBDMS) protecting group enhances stability and selectivity during reactions, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The compound is also utilized in th

This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a boronic ester reagent, enabling the formation of carbon-carbon bonds in the presence of a palladium catalyst. Its tert-butyldimethylsilyl (TBDMS) protecting group enhances stability and selectivity during reactions, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The compound is also utilized in the development of advanced materials and fine chemicals, where precise control over molecular structure is essential. Its application is favored in research and industrial settings for its efficiency and reliability in creating diverse chemical architectures.

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