(E)-3-(tert-Butyldimethylsilyloxy)propene-1-yl-boronic acid pinacol ester

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Reagent Code: #89399
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CAS Number 114653-19-9

science Other reagents with same CAS 114653-19-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 298.3 g/mol
Formula C₁₅H₃₁BO₃Si
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MDL Number MFCD15144803
inventory_2 Storage & Handling
Storage room temperature, dry

description Product Description

This chemical is widely used as a key intermediate in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. It enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its tert-butyldimethylsilyl (TBDMS) protecting group enhances stability during reactions, allowing for selective transformations. Additionally, it is employed in the preparation of functionalized alkenes and other boron-containing compounds, which are essential in medicinal chemistry and material science research.

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Test Parameter Specification
Appearance Light yellow liquid
Purity (%) 94.5-100
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,990.00

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(E)-3-(tert-Butyldimethylsilyloxy)propene-1-yl-boronic acid pinacol ester
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This chemical is widely used as a key intermediate in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. It enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its tert-butyldimethylsilyl (TBDMS) protecting group enhances stability during reactions, allowing for selective transformations. Additionally, it is employed in the preparation of

This chemical is widely used as a key intermediate in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. It enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. Its tert-butyldimethylsilyl (TBDMS) protecting group enhances stability during reactions, allowing for selective transformations. Additionally, it is employed in the preparation of functionalized alkenes and other boron-containing compounds, which are essential in medicinal chemistry and material science research.

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