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

98%

Reagent Code: #201023
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CAS Number 848243-25-4

science Other reagents with same CAS 848243-25-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 263.14 g/mol
Formula C₁₄H₂₂BNO₃
badge Registry Numbers
MDL Number MFCD07366722
inventory_2 Storage & Handling
Storage -20°C, Sealed, Drying, Inert Gas

description Product Description

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates efficient coupling with aryl or heteroaryl halides under palladium catalysis, making it valuable in the development of complex organic molecules, particularly in drug discovery and materials science. The isopropoxy group enhances stability and influences reactivity, improving selectivity in coupling processes.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿640.00
inventory 1g
10-20 days ฿1,940.00
inventory 5g
10-20 days ฿6,380.00
2-Isopropoxy-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
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Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates efficient coupling with aryl or heteroaryl halides under palladium catalysis, making it valuable in the development of complex organic molecules, particularly in drug discovery and materials science. The isopropoxy group enhances stability and influences reactivity, improving selectivity in coupling processe

Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its boronate ester group facilitates efficient coupling with aryl or heteroaryl halides under palladium catalysis, making it valuable in the development of complex organic molecules, particularly in drug discovery and materials science. The isopropoxy group enhances stability and influences reactivity, improving selectivity in coupling processes.

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