2-Chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde

98%

Reagent Code: #164799
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CAS Number 1356401-39-2

science Other reagents with same CAS 1356401-39-2

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inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used primarily as a building block in Suzuki-Miyaura cross-coupling reactions, this compound enables the synthesis of complex aromatic aldehydes and biaryl structures. Its boronate ester group readily participates in palladium-catalyzed couplings, making it valuable in pharmaceutical and agrochemical research for constructing carbon-carbon bonds. The aldehyde functionality allows further derivatization, such as reduction to alcohols, conversion to imines, or use in condensation reactions, adding versatility in multi-step organic synthesis. It is especially useful in the development of functionalized aromatic systems for materials science and drug discovery.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,700.00
inventory 250mg
10-20 days ฿9,740.00
inventory 1g
10-20 days ฿26,430.00
inventory 5g
10-20 days ฿87,440.00

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2-Chloro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde
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Used primarily as a building block in Suzuki-Miyaura cross-coupling reactions, this compound enables the synthesis of complex aromatic aldehydes and biaryl structures. Its boronate ester group readily participates in palladium-catalyzed couplings, making it valuable in pharmaceutical and agrochemical research for constructing carbon-carbon bonds. The aldehyde functionality allows further derivatization, such as reduction to alcohols, conversion to imines, or use in condensation reactions, adding versatil

Used primarily as a building block in Suzuki-Miyaura cross-coupling reactions, this compound enables the synthesis of complex aromatic aldehydes and biaryl structures. Its boronate ester group readily participates in palladium-catalyzed couplings, making it valuable in pharmaceutical and agrochemical research for constructing carbon-carbon bonds. The aldehyde functionality allows further derivatization, such as reduction to alcohols, conversion to imines, or use in condensation reactions, adding versatility in multi-step organic synthesis. It is especially useful in the development of functionalized aromatic systems for materials science and drug discovery.

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