5-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-3,4-dihydroquinolin-2(1H)-one
95%
Reagent
Code: #243482
CAS Number
2446617-95-2
blur_circular Chemical Specifications
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Molecular Information
Weight
273.14 g/mol
Formula
C₁₅H₂₀BNO₃
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Storage & Handling
Storage
2-8°C, dry
description Product Description
Used primarily in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions. It enables the formation of carbon-carbon bonds, particularly in the construction of biaryl or heterobiaryl systems found in pharmaceuticals and agrochemicals. The compound’s dihydroquinolinone core provides a scaffold useful in drug discovery, while the boronate group allows for efficient and selective coupling under mild palladium catalysis. It is especially valuable in the development of bioactive molecules and functional materials requiring precise molecular architecture.
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