4-Benzyloxy-2-formylphenylboronic Acid

95%, containing varying amounts of acid anhydrides

Reagent Code: #90731
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CAS Number 139962-97-3

science Other reagents with same CAS 139962-97-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 256.06 g/mol
Formula C₁₄H₁₃BO₄
badge Registry Numbers
MDL Number MFCD02179486
inventory_2 Storage & Handling
Storage room temperature, in an inert gas

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of complex molecules, particularly in Suzuki-Miyaura cross-coupling reactions. It facilitates the formation of carbon-carbon bonds, enabling the construction of biaryl structures, which are prevalent in pharmaceuticals and agrochemicals. Its boronic acid group is essential for coupling with aryl halides, while the formyl group offers a reactive site for further functionalization. This makes it valuable in the development of drug candidates and advanced materials. Additionally, its benzyloxy group provides protection for phenolic hydroxyl groups during multi-step synthetic processes.

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Size Availability Unit Price Quantity
inventory 200mg
10-20 days ฿6,462.00

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4-Benzyloxy-2-formylphenylboronic Acid
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Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of complex molecules, particularly in Suzuki-Miyaura cross-coupling reactions. It facilitates the formation of carbon-carbon bonds, enabling the construction of biaryl structures, which are prevalent in pharmaceuticals and agrochemicals. Its boronic acid group is essential for coupling with aryl halides, while the formyl group offers a reactive site for further functionalization. This makes it valuable in t

Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of complex molecules, particularly in Suzuki-Miyaura cross-coupling reactions. It facilitates the formation of carbon-carbon bonds, enabling the construction of biaryl structures, which are prevalent in pharmaceuticals and agrochemicals. Its boronic acid group is essential for coupling with aryl halides, while the formyl group offers a reactive site for further functionalization. This makes it valuable in the development of drug candidates and advanced materials. Additionally, its benzyloxy group provides protection for phenolic hydroxyl groups during multi-step synthetic processes.

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