4,4,5,5-tetramethyl-2-[2-(phenoxymethyl)phenyl]-1,3,2-dioxaborolane

95%

Reagent Code: #89709
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CAS Number 912569-55-2

science Other reagents with same CAS 912569-55-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 310.1951 g/mol
Formula C₁₉H₂₃BO₃
badge Registry Numbers
MDL Number MFCD09064986
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its boronic ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, it can serve as a key building block in the development of boron-containing compounds, which are often explored for their potential in drug discovery and material science. Its stability and reactivity make it suitable for use in controlled reactions, ensuring high yields and specificity in the production of target molecules.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿2,925.00
inventory 250mg
10-20 days ฿11,700.00

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4,4,5,5-tetramethyl-2-[2-(phenoxymethyl)phenyl]-1,3,2-dioxaborolane
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This chemical is primarily used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its boronic ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, it can serve as a key building block in the development of boron-containing compounds, which are often explored for their potential in drug discovery and

This chemical is primarily used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its boronic ester functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to form carbon-carbon bonds in the synthesis of complex organic molecules. Additionally, it can serve as a key building block in the development of boron-containing compounds, which are often explored for their potential in drug discovery and material science. Its stability and reactivity make it suitable for use in controlled reactions, ensuring high yields and specificity in the production of target molecules.

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