tert-Butyl(4-fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)dimethylsilane

97%

Reagent Code: #130421
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CAS Number 2377611-08-8

science Other reagents with same CAS 2377611-08-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 352.32 g/mol
Formula C₁₈H₃₀BFO₃Si
badge Registry Numbers
MDL Number MFCD28515403
thermostat Physical Properties
Boiling Point 387.8±32.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.00±0.1 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used primarily as a specialized intermediate in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronate ester group enables the formation of carbon-carbon bonds, making it valuable in the construction of biaryl and substituted aromatic systems found in pharmaceuticals and agrochemicals. The tert-butyldimethylsilyl (TBS) protected phenoxy group provides stability and selectivity during multi-step syntheses, allowing for controlled deprotection under mild conditions. This compound is especially useful in the development of complex molecules where orthogonal protection and functional group compatibility are required.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿4,500.00
inventory 1g
10-20 days ฿12,000.00

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tert-Butyl(4-fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenoxy)dimethylsilane
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Used primarily as a specialized intermediate in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronate ester group enables the formation of carbon-carbon bonds, making it valuable in the construction of biaryl and substituted aromatic systems found in pharmaceuticals and agrochemicals. The tert-butyldimethylsilyl (TBS) protected phenoxy group provides stability and selectivity during multi-step syntheses, allowing for controlled deprotection under mild c

Used primarily as a specialized intermediate in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronate ester group enables the formation of carbon-carbon bonds, making it valuable in the construction of biaryl and substituted aromatic systems found in pharmaceuticals and agrochemicals. The tert-butyldimethylsilyl (TBS) protected phenoxy group provides stability and selectivity during multi-step syntheses, allowing for controlled deprotection under mild conditions. This compound is especially useful in the development of complex molecules where orthogonal protection and functional group compatibility are required.

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