7-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)quinoline
97%
Reagent
Code: #242717
CAS Number
851985-81-4
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
MFCD08063115
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Storage & Handling
Storage
2-8°C, dry, sealed
description Product Description
Used as a key intermediate in Suzuki-Miyaura cross-coupling reactions, enabling the synthesis of complex quinoline derivatives with pharmaceutical and agrochemical relevance. Its boronate ester group facilitates mild, selective bond formation with aryl halides, making it valuable in drug discovery and materials science. Commonly applied in the preparation of fluorescent probes and organic semiconductors due to the quinoline core’s electronic properties. Also utilized in medicinal chemistry for constructing libraries of bioactive molecules targeting kinases and other enzymes.
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