2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-5-(trifluoromethyl)benzaldehyde

98%

Reagent Code: #243006
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CAS Number 1219936-17-0

science Other reagents with same CAS 1219936-17-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 300.08 g/mol
Formula C₁₄H₁₆BF₃O₃
badge Registry Numbers
MDL Number MFCD18383807
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 coupling with aryl halides, making it valuable in pharmaceutical and agrochemical research for developing fluorinated compounds. The presence of both aldehyde and trifluoromethyl groups allows further functionalization, enabling diverse molecular transformations. It is especially useful in the synthesis of bioactive molecules where the trifluoromethyl group enhances metabolic stability and lipophilicity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿980.00
inventory 250mg
10-20 days ฿1,740.00
inventory 1g
10-20 days ฿4,690.00
inventory 25g
10-20 days ฿71,710.00
inventory 5g
10-20 days ฿14,360.00

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2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-5-(trifluoromethyl)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 coupling with aryl halides, making it valuable in pharmaceutical and agrochemical research for developing fluorinated compounds. The presence of both aldehyde and trifluoromethyl groups allows further functionalization, enabling diverse molecular transformations. It is especially useful in the synthesis of bioactive molecules where the trifluoromethyl group enhances metabolic stability and lipophilicity.
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