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

95%

Reagent Code: #167200
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CAS Number 1331943-76-0

science Other reagents with same CAS 1331943-76-0

blur_circular Chemical Specifications

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Weight 268.06 g/mol
Formula C₁₃H₁₅BF₂O₃
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 or vinyl halides, making it valuable in pharmaceutical and agrochemical research. The presence of fluorine atoms enhances reactivity and influences electronic properties, which can improve the metabolic stability and bioavailability of target molecules. It is especially useful in the development of fluorinated drug candidates and functional materials where precise molecular design is critical.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,920.00
inventory 250mg
10-20 days ฿6,660.00
inventory 1g
10-20 days ฿17,970.00

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2,3-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 or vinyl halides, making it valuable in pharmaceutical and agrochemical research. The presence of fluorine atoms enhances reactivity and influences electronic properties, which can improve the metabolic stability and bioavailability of target molec

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 or vinyl halides, making it valuable in pharmaceutical and agrochemical research. The presence of fluorine atoms enhances reactivity and influences electronic properties, which can improve the metabolic stability and bioavailability of target molecules. It is especially useful in the development of fluorinated drug candidates and functional materials where precise molecular design is critical.

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