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.

Available Sizes & Pricing

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