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

97%

Reagent Code: #206622
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CAS Number 1012084-56-8

science Other reagents with same CAS 1012084-56-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 219.09 g/mol
Formula C₁₂H₁₈BNO₂
badge Registry Numbers
MDL Number MFCD08669594
thermostat Physical Properties
Boiling Point 311.6±30.0°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Widely used in cross-coupling reactions, especially in Suzuki-Miyaura coupling, to introduce substituted pyridine moieties into organic molecules. Its boronate ester group readily reacts with aryl or heteroaryl halides in the presence of palladium catalysts, enabling the synthesis of complex pyridine-based structures. Commonly applied in pharmaceutical development, agrochemicals, and materials science where functionalized pyridines enhance biological activity or electronic properties. Stable and easy to handle, it serves as a valuable building block in medicinal chemistry for constructing drug candidates targeting various diseases.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿1,090.00
5g
10-20 days ฿5,040.00
10g
10-20 days ฿10,000.00
25g
10-20 days ฿24,630.00
100g
10-20 days ฿86,400.00
2-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
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Widely used in cross-coupling reactions, especially in Suzuki-Miyaura coupling, to introduce substituted pyridine moieties into organic molecules. Its boronate ester group readily reacts with aryl or heteroaryl halides in the presence of palladium catalysts, enabling the synthesis of complex pyridine-based structures. Commonly applied in pharmaceutical development, agrochemicals, and materials science where functionalized pyridines enhance biological activity or electronic properties. Stable and easy to

Widely used in cross-coupling reactions, especially in Suzuki-Miyaura coupling, to introduce substituted pyridine moieties into organic molecules. Its boronate ester group readily reacts with aryl or heteroaryl halides in the presence of palladium catalysts, enabling the synthesis of complex pyridine-based structures. Commonly applied in pharmaceutical development, agrochemicals, and materials science where functionalized pyridines enhance biological activity or electronic properties. Stable and easy to handle, it serves as a valuable building block in medicinal chemistry for constructing drug candidates targeting various diseases.

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