4,4,5,5-Tetramethyl-2-(2-((4-methylbenzyl)oxy)phenyl)-1,3,2-dioxaborolane

98%

Reagent Code: #242865
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CAS Number 2246645-45-2

science Other reagents with same CAS 2246645-45-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 324.22 g/mol
Formula C₂₀H₂₅BO₃
thermostat Physical Properties
Boiling Point 449.5±33.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.07±0.1 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Particularly valuable in pharmaceutical and agrochemical industries for constructing biaryl compounds. Its electron-rich borolane structure enhances coupling efficiency and stability under mild reaction conditions. Also employed in the development of organic electronic materials due to its ability to support conjugated frameworks.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿9,300.00
inventory 1g
10-20 days ฿23,250.00
inventory 100mg
10-20 days ฿5,550.00

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4,4,5,5-Tetramethyl-2-(2-((4-methylbenzyl)oxy)phenyl)-1,3,2-dioxaborolane
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Particularly valuable in pharmaceutical and agrochemical industries for constructing biaryl compounds. Its electron-rich borolane structure enhances coupling efficiency and stability under mild reaction conditions. Also employed in the development of organic electronic materials due to its ability to support conjugated frameworks.

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Particularly valuable in pharmaceutical and agrochemical industries for constructing biaryl compounds. Its electron-rich borolane structure enhances coupling efficiency and stability under mild reaction conditions. Also employed in the development of organic electronic materials due to its ability to support conjugated frameworks.

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