3-[2-(Trimethylsilyl)ethynyl]benzeneboronic acid pinacol ester

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Reagent Code: #90106
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CAS Number 915402-03-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 300.28 g/mol
Formula C₁₇H₂₅BO₂Si
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MDL Number MFCD08706285
inventory_2 Storage & Handling
Storage 2-8°C, airtight, dry

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its structure, featuring a boronic ester group and a trimethylsilyl-protected alkyne, makes it a versatile building block for constructing complex molecules. The boronic ester moiety facilitates the formation of carbon-carbon bonds with aryl or vinyl halides, while the protected alkyne can be deprotected and further functionalized. This chemical is valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials, where precise control over molecular architecture is required. Its stability and reactivity under mild conditions make it a preferred choice in modern synthetic chemistry.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,780.00
3-[2-(Trimethylsilyl)ethynyl]benzeneboronic acid pinacol ester
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its structure, featuring a boronic ester group and a trimethylsilyl-protected alkyne, makes it a versatile building block for constructing complex molecules. The boronic ester moiety facilitates the formation of carbon-carbon bonds with aryl or vinyl halides, while the protected alkyne can be deprotected and further functionalized. This chemical is valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials, where precise control over molecular architecture is required. Its stability and reactivity under mild conditions make it a preferred choice in modern synthetic chemistry.
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