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

97%

Reagent Code: #148681
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CAS Number 458532-92-8

science Other reagents with same CAS 458532-92-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 283.96 g/mol
Formula C₁₁H₁₅BBrNO₂
badge Registry Numbers
MDL Number MFCD06798250
thermostat Physical Properties
Boiling Point 340.6°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Used primarily in cross-coupling reactions, this compound serves as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables Suzuki-Miyaura coupling, allowing efficient formation of carbon-carbon bonds with aryl or heteroaryl halides. This makes it valuable in constructing complex nitrogen-containing heterocycles found in bioactive molecules. It is also employed in materials science for creating organic semiconductors and functional polymers due to its ability to introduce pyridine moieties into larger conjugated systems.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,970.00
inventory 1g
10-20 days ฿6,680.00
inventory 5g
10-20 days ฿27,730.00

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3-Bromo-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
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Used primarily in cross-coupling reactions, this compound serves as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables Suzuki-Miyaura coupling, allowing efficient formation of carbon-carbon bonds with aryl or heteroaryl halides. This makes it valuable in constructing complex nitrogen-containing heterocycles found in bioactive molecules. It is also employed in materials science for creating organic semiconductors and functional polymers due to its ab

Used primarily in cross-coupling reactions, this compound serves as a key intermediate in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables Suzuki-Miyaura coupling, allowing efficient formation of carbon-carbon bonds with aryl or heteroaryl halides. This makes it valuable in constructing complex nitrogen-containing heterocycles found in bioactive molecules. It is also employed in materials science for creating organic semiconductors and functional polymers due to its ability to introduce pyridine moieties into larger conjugated systems.

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