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

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Reagent Code: #244097
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CAS Number 878194-93-5

science Other reagents with same CAS 878194-93-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 230.07 g/mol
Formula C₁₂H₁₅BN₂O₂
badge Registry Numbers
MDL Number MFCD08458477
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, inert gas

description Product Description

Used primarily in cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient Suzuki-Miyaura coupling, allowing for the formation of biaryl and heteroaryl structures commonly found in bioactive molecules. The nitrile group adds further functionality, enabling additional transformations such as hydrolysis to carboxylic acids or reduction to amines. It is especially valuable in medicinal chemistry for constructing complex nitrogen-containing heterocycles with high selectivity and yield.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,990.00
inventory 1g
10-20 days ฿6,380.00
inventory 5g
10-20 days ฿23,940.00
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3-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)picolinonitrile
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Used primarily in cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boronate ester group enables efficient Suzuki-Miyaura coupling, allowing for the formation of biaryl and heteroaryl structures commonly found in bioactive molecules. The nitrile group adds further functionality, enabling additional transformations such as hydrolysis to carboxylic acids or reduction to amines. It is especially valuable in medicinal chemistry for constructing complex nitrogen-containing heterocycles with high selectivity and yield.
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