2-(Difluoromethoxy)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine

95%

Reagent Code: #41880
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CAS Number 1628116-87-9

science Other reagents with same CAS 1628116-87-9

blur_circular Chemical Specifications

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Weight 271.07 g/mol
Formula C₁₂H₁₆BF₂NO₃
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. Its boronate ester group enables it to act as a key intermediate in the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, its pyridine moiety can serve as a directing group in metal-catalyzed reactions, further expanding its utility in constructing heterocyclic compounds. The difluoromethoxy group enhances its stability and reactivity, making it suitable for applications in drug discovery and material science.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,779.00
inventory 250mg
10-20 days ฿9,567.00

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2-(Difluoromethoxy)-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronate ester group enables it to act as a key intermediate in the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, its pyridine moiety can serve as a directing group in metal-catalyzed reactions, further expanding its utility in constructing heterocyclic compou

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronate ester group enables it to act as a key intermediate in the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, its pyridine moiety can serve as a directing group in metal-catalyzed reactions, further expanding its utility in constructing heterocyclic compounds. The difluoromethoxy group enhances its stability and reactivity, making it suitable for applications in drug discovery and material science.

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