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

scatter_plot Molecular Information
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.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿4,779.00
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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