4-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenylethynyl-trimethylsilane

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Reagent Code: #118789
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CAS Number 870238-65-6

science Other reagents with same CAS 870238-65-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 300.28 g/mol
Formula C₁₇H₂₅BO₂Si
badge Registry Numbers
MDL Number MFCD08706286
inventory_2 Storage & Handling
Storage Room temperature, dry, sealed

description Product Description

This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group makes it a valuable intermediate for constructing complex organic molecules, especially in the pharmaceutical and materials science fields. The phenylethynyl group allows for further functionalization, enabling the creation of conjugated systems, which are essential in developing organic electronic materials like OLEDs and semiconductors. Additionally, the trimethylsilyl group provides stability and can be selectively removed or transformed, offering versatility in synthetic pathways.

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Test Parameter Specification
APPEARANCE White to Cream to Yellow Solid
Purity (%) 96.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿9,369.00
inventory 5g
10-20 days ฿40,113.00

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4-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenylethynyl-trimethylsilane
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This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group makes it a valuable intermediate for constructing complex organic molecules, especially in the pharmaceutical and materials science fields. The phenylethynyl group allows for further functionalization, enabling the creation of conjugated systems, which are essential in developing organic electronic materials like OLEDs and semiconductors. Additionall

This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronate ester group makes it a valuable intermediate for constructing complex organic molecules, especially in the pharmaceutical and materials science fields. The phenylethynyl group allows for further functionalization, enabling the creation of conjugated systems, which are essential in developing organic electronic materials like OLEDs and semiconductors. Additionally, the trimethylsilyl group provides stability and can be selectively removed or transformed, offering versatility in synthetic pathways.

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