2-(4-(Difluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

≥95%

Reagent Code: #118681
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CAS Number 1234319-14-2

science Other reagents with same CAS 1234319-14-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 254.08 g/mol
Formula C₁₃H₁₇BF₂O₂
badge Registry Numbers
MDL Number MFCD16996278
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a boronic ester reagent, enabling the formation of carbon-carbon bonds, which is essential in constructing complex organic molecules. Its difluoromethylphenyl group enhances reactivity and selectivity, making it valuable in pharmaceutical research for developing drug candidates. Additionally, it is employed in material science for creating advanced polymers and functional materials with specific electronic or optical properties.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿10,431.00
inventory 100mg
10-20 days ฿882.00
inventory 1g
10-20 days ฿2,898.00
inventory 250mg
10-20 days ฿1,152.00

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2-(4-(Difluoromethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a boronic ester reagent, enabling the formation of carbon-carbon bonds, which is essential in constructing complex organic molecules. Its difluoromethylphenyl group enhances reactivity and selectivity, making it valuable in pharmaceutical research for developing drug candidates. Additionally, it is employed in material science for creating advanced polymers and

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a boronic ester reagent, enabling the formation of carbon-carbon bonds, which is essential in constructing complex organic molecules. Its difluoromethylphenyl group enhances reactivity and selectivity, making it valuable in pharmaceutical research for developing drug candidates. Additionally, it is employed in material science for creating advanced polymers and functional materials with specific electronic or optical properties.

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