2-Phenoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
98%
Reagent
Code: #89887
CAS Number
330792-76-2
science Other reagents with same CAS 330792-76-2
blur_circular Chemical Specifications
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Molecular Information
Weight
297.16 g/mol
Formula
C₁₇H₂₀BNO₃
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Storage & Handling
Storage
2-8°C
description Product Description
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions. It serves as a key intermediate in the formation of carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronate ester group makes it valuable in Suzuki-Miyaura coupling reactions, which are widely employed in pharmaceutical and material science research. Additionally, it finds application in the development of advanced materials, such as organic semiconductors and liquid crystals, due to its ability to introduce specific functional groups into molecular structures. Its stability and reactivity also make it suitable for use in medicinal chemistry for the synthesis of biologically active compounds.
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