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

97%

Reagent Code: #240841
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CAS Number 929203-04-3

science Other reagents with same CAS 929203-04-3

blur_circular Chemical Specifications

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Weight 281.16 g/mol
Formula C₁₇H₂₀BNO₂
inventory_2 Storage & Handling
Storage 2-8°C

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 boron-containing group enables efficient Suzuki-Miyaura coupling, allowing the formation of biaryl structures that are common in active pharmaceutical ingredients. It is also employed in the development of organic electronic materials, such as OLEDs and semiconductors, due to its ability to modify electron transport properties. The pyridine ring enhances binding selectivity in medicinal chemistry applications, making it valuable in drug discovery for targeting specific enzymes or receptors.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿170.50
inventory 1g
10-20 days ฿462.00
inventory 5g
10-20 days ฿1,771.00

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3-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyridine
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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 boron-containing group enables efficient Suzuki-Miyaura coupling, allowing the formation of biaryl structures that are common in active pharmaceutical ingredients. It is also employed in the development of organic electronic materials, such as OLEDs and semiconductors, due to its ability to modify electron transport properties. The pyridine ring enhances bind

Used primarily in cross-coupling reactions, this compound serves as a key building block in the synthesis of pharmaceuticals and agrochemicals. Its boron-containing group enables efficient Suzuki-Miyaura coupling, allowing the formation of biaryl structures that are common in active pharmaceutical ingredients. It is also employed in the development of organic electronic materials, such as OLEDs and semiconductors, due to its ability to modify electron transport properties. The pyridine ring enhances binding selectivity in medicinal chemistry applications, making it valuable in drug discovery for targeting specific enzymes or receptors.

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