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

95%

Reagent Code: #41445
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CAS Number 1648930-13-5

science Other reagents with same CAS 1648930-13-5

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Weight 328.1855832 g/mol
Formula C₁₉H₂₂BFO₃
inventory_2 Storage & Handling
Storage 2-8℃

description Product Description

This chemical 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 the production of pharmaceuticals, agrochemicals, and advanced materials. Its structure, featuring a fluorophenoxy group, enhances its reactivity and selectivity in these reactions, making it valuable for constructing complex organic molecules. Additionally, it is employed in the development of boron-based compounds for potential use in medicinal chemistry and material science research.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿10,593.00
inventory 1g
10-20 days ฿25,650.00
inventory 100mg
10-20 days ฿6,354.00

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2-(3-((4-Fluorophenoxy)methyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
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This chemical 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 the production of pharmaceuticals, agrochemicals, and advanced materials. Its structure, featuring a fluorophenoxy group, enhances its reactivity and selectivity in these reactions, making it valuable for constructing complex organic molecules. Additionally, it is emplo

This chemical 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 the production of pharmaceuticals, agrochemicals, and advanced materials. Its structure, featuring a fluorophenoxy group, enhances its reactivity and selectivity in these reactions, making it valuable for constructing complex organic molecules. Additionally, it is employed in the development of boron-based compounds for potential use in medicinal chemistry and material science research.

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