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

≥95%

Reagent Code: #116062
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CAS Number 960067-33-8

science Other reagents with same CAS 960067-33-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 270.08 g/mol
Formula C₁₃H₁₇BF₂O₃
badge Registry Numbers
MDL Number MFCD16996403
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It acts as a boronic ester reagent, facilitating the formation of carbon-carbon bonds between aryl or vinyl boronic acids and aryl or vinyl halides. This makes it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity under mild conditions make it a preferred choice for constructing complex organic molecules. Additionally, it is employed in the development of electronic materials and polymers, where precise molecular structures are critical for performance.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,754.00

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2-(2-(Difluoromethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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This compound is primarily used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It acts as a boronic ester reagent, facilitating the formation of carbon-carbon bonds between aryl or vinyl boronic acids and aryl or vinyl halides. This makes it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity under mild conditions make it a preferred choice for constructing complex organic molecules. Additionally, it is employed in the development of electronic materials and polymers, where precise molecular structures are critical for performance.
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