5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-ol

97%

Reagent Code: #241728
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CAS Number 1054483-78-1

science Other reagents with same CAS 1054483-78-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 221.06 g/mol
Formula C₁₁H₁₆BNO₃
badge Registry Numbers
MDL Number MFCD06795671
inventory_2 Storage & Handling
Storage 2-8°C, stored in inert gas

description Product Description

Widely used in cross-coupling reactions, particularly in Suzuki-Miyaura coupling, this compound serves as a key building block for constructing biaryl and heteroaryl frameworks in pharmaceutical and agrochemical synthesis. Its boronate ester group readily participates in palladium-catalyzed reactions with aryl or heteroaryl halides, enabling efficient formation of carbon-carbon bonds. The presence of a hydroxyl group on the pyridine ring offers an additional site for functionalization or coordination, making it valuable in ligand design and metal-organic frameworks. It is also employed in the development of organic electronic materials due to its ability to tune electronic properties in conjugated systems.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿462.00
inventory 1g
10-20 days ฿1,710.00

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5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)pyridin-2-ol
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Widely used in cross-coupling reactions, particularly in Suzuki-Miyaura coupling, this compound serves as a key building block for constructing biaryl and heteroaryl frameworks in pharmaceutical and agrochemical synthesis. Its boronate ester group readily participates in palladium-catalyzed reactions with aryl or heteroaryl halides, enabling efficient formation of carbon-carbon bonds. The presence of a hydroxyl group on the pyridine ring offers an additional site for functionalization or coordination, ma

Widely used in cross-coupling reactions, particularly in Suzuki-Miyaura coupling, this compound serves as a key building block for constructing biaryl and heteroaryl frameworks in pharmaceutical and agrochemical synthesis. Its boronate ester group readily participates in palladium-catalyzed reactions with aryl or heteroaryl halides, enabling efficient formation of carbon-carbon bonds. The presence of a hydroxyl group on the pyridine ring offers an additional site for functionalization or coordination, making it valuable in ligand design and metal-organic frameworks. It is also employed in the development of organic electronic materials due to its ability to tune electronic properties in conjugated systems.

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