2-Phenyl-7-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline
97%
Reagent
Code: #226311
CAS Number
867164-54-3
blur_circular Chemical Specifications
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Molecular Information
Weight
331.22 g/mol
Formula
C₂₁H₂₂BNO₂
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Registry Numbers
MDL Number
MFCD22126087
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Storage & Handling
Storage
2-8°C, stored in inert gas
description Product Description
Used primarily in organic synthesis as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. Its boronate ester group facilitates coupling with aryl or heteroaryl halides, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials such as organic light-emitting diodes (OLEDs). The quinoline core provides structural stability and electronic properties useful in designing functional molecules. Its application is especially prominent in medicinal chemistry for constructing complex aromatic systems.
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