3-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)pyridine
97%
Reagent
Code: #240841
CAS Number
929203-04-3
blur_circular Chemical Specifications
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Molecular Information
Weight
281.16 g/mol
Formula
C₁₇H₂₀BNO₂
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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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