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

97%

Reagent Code: #117698
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CAS Number 1112209-24-1

science Other reagents with same CAS 1112209-24-1

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scatter_plot Molecular Information
Weight 250.07 g/mol
Formula C₁₃H₁₆BFO₃
badge Registry Numbers
MDL Number MFCD16996301
inventory_2 Storage & Handling
Storage 2-8°C, inert gas

description Product Description

This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate in the production of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. The presence of the boronate ester group makes it highly reactive and suitable for forming carbon-carbon bonds, which is essential in constructing diverse molecular structures. Additionally, its aldehyde functionality allows for further derivatization, enabling the synthesis of a wide range of compounds with potential biological or industrial applications. Its use is particularly prominent in medicinal chemistry for designing drug candidates and in material science for developing functional polymers and organic electronic materials.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,339.00
inventory 1g
10-20 days ฿9,000.00
inventory 100mg
10-20 days ฿1,971.00

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3-Fluoro-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde
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This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate in the production of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. The presence of the boronate ester group makes it highly reactive and suitable for forming carbon-carbon bonds, which is essential in constructing diverse molecular structures. Additionally, its aldehyde functionality allows for furthe

This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate in the production of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. The presence of the boronate ester group makes it highly reactive and suitable for forming carbon-carbon bonds, which is essential in constructing diverse molecular structures. Additionally, its aldehyde functionality allows for further derivatization, enabling the synthesis of a wide range of compounds with potential biological or industrial applications. Its use is particularly prominent in medicinal chemistry for designing drug candidates and in material science for developing functional polymers and organic electronic materials.

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