2,6-Difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde

97%

Reagent Code: #168468
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CAS Number 2088247-40-7

science Other reagents with same CAS 2088247-40-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 268.06 g/mol
Formula C₁₃H₁₅BF₂O₃
badge Registry Numbers
MDL Number MFCD17215216
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

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 complex aromatic systems. Its boronate ester group enables efficient carbon-carbon bond formation with aryl halides, making it valuable in pharmaceutical and agrochemical research. The aldehyde functionality allows further derivatization, such as reduction to alcohols, conversion to imines, or participation in condensation reactions. This dual reactivity makes it a versatile intermediate in the development of bioactive molecules and functional materials.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,010.00
inventory 1g
10-20 days ฿4,150.00
inventory 5g
10-20 days ฿14,610.00
inventory 250mg
10-20 days ฿1,660.00

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2,6-Difluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde
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Widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key building block for constructing complex aromatic systems. Its boronate ester group enables efficient carbon-carbon bond formation with aryl halides, making it valuable in pharmaceutical and agrochemical research. The aldehyde functionality allows further derivatization, such as reduction to alcohols, conversion to imines, or participation in condensation reactions. This dual reactivity makes it a versatile intermediate in the development of bioactive molecules and functional materials.
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