4-(4,4,5,5-Tetramethyl-[1,3,2]dioxaborolan-2-yl)quinoline
95%
Reagent
Code: #240852
CAS Number
1035458-54-8
blur_circular Chemical Specifications
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Molecular Information
Weight
255.12 g/mol
Formula
C₁₅H₁₈BNO₂
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Registry Numbers
MDL Number
MFCD05155221
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Storage & Handling
Storage
2-8°C
description Product Description
Used in Suzuki-Miyaura cross-coupling reactions to synthesize complex quinoline derivatives, which are important in pharmaceutical and agrochemical industries. Its boronate ester group enables efficient carbon-carbon bond formation under mild conditions. Commonly applied in the development of bioactive molecules, organic semiconductors, and fluorescent probes due to the quinoline moiety’s electron-accepting properties. Also utilized in materials science for constructing conjugated systems in OLEDs and sensors.
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