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

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Reagent Code: #118527
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CAS Number 864754-47-2

science Other reagents with same CAS 864754-47-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 266.12 g/mol
Formula C₁₄H₂₀BFO₃
badge Registry Numbers
MDL Number MFCD08706126
thermostat Physical Properties
Boiling Point 352.3±27.0°C at 760 mmHg
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 Suzuki-Miyaura cross-coupling reactions. Its boronate ester group acts as a key intermediate, enabling the formation of carbon-carbon bonds between aryl or vinyl boronic acids and aryl or vinyl halides. This reaction is widely applied in the pharmaceutical industry for the synthesis of complex molecules, including drug candidates and bioactive compounds. Additionally, the fluorine-containing ethoxy group enhances its stability and reactivity, making it suitable for use in advanced material science, such as the development of organic electronic materials and polymers. Its unique structure also allows for potential applications in the design of fluorescent probes and imaging agents in biochemical research.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,663.00
inventory 1g
10-20 days ฿9,153.00
inventory 5g
10-20 days ฿29,277.00
inventory 100mg
10-20 days ฿2,439.00

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2-(4-(2-Fluoroethoxy)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its boronate ester group acts as a key intermediate, enabling the formation of carbon-carbon bonds between aryl or vinyl boronic acids and aryl or vinyl halides. This reaction is widely applied in the pharmaceutical industry for the synthesis of complex molecules, including drug candidates and bioactive compounds. Additionally, the fluorine-containing ethoxy group enhances its stability and

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. Its boronate ester group acts as a key intermediate, enabling the formation of carbon-carbon bonds between aryl or vinyl boronic acids and aryl or vinyl halides. This reaction is widely applied in the pharmaceutical industry for the synthesis of complex molecules, including drug candidates and bioactive compounds. Additionally, the fluorine-containing ethoxy group enhances its stability and reactivity, making it suitable for use in advanced material science, such as the development of organic electronic materials and polymers. Its unique structure also allows for potential applications in the design of fluorescent probes and imaging agents in biochemical research.

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