4’-(4,4,5,5-Tetramethyl-1,3,2-Dioxaborolan-2-Yl)-[1,1’-Biphenyl]-4-Carbaldehyde
97%
Reagent
Code: #243941
CAS Number
1040424-52-9
blur_circular Chemical Specifications
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Molecular Information
Weight
308.18 g/mol
Formula
C₁₉H₂₁BO₃
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Storage & Handling
Storage
Room temperature
description Product Description
Widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block for constructing biaryl frameworks found in pharmaceuticals, agrochemicals, and advanced materials. The boronate ester group enables efficient coupling with aryl halides under palladium catalysis, while the aldehyde functionality allows for further derivatization, such as condensation reactions or reduction to alcohols. Its dual functional groups make it valuable in the development of complex organic molecules, including liquid crystals, organic semiconductors, and drug intermediates. It is also employed in the synthesis of conjugated polymers and metal-organic frameworks due to its structural rigidity and reactivity.
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