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

98%

Reagent Code: #118912
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CAS Number 1112208-82-8

science Other reagents with same CAS 1112208-82-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 250.07 g/mol
Formula C₁₃H₁₆BFO₃
badge Registry Numbers
MDL Number MFCD11867877
thermostat Physical Properties
Boiling Point 350.0±32.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.12±0.1 g/cm3(Predicted)
Storage 2-8°C, inert gas

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a key intermediate for constructing complex molecules. Its boronate ester group facilitates the formation of carbon-carbon bonds, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the synthesis of fluorinated aromatic compounds, which are often used in drug discovery due to their enhanced metabolic stability and bioavailability. Its applications also extend to material science, where it contributes to the creation of organic electronic components and polymers with specific properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,934.00
inventory 1g
10-20 days ฿7,920.00
inventory 100mg
10-20 days ฿1,737.00

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4-Fluoro-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzaldehyde
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a key intermediate for constructing complex molecules. Its boronate ester group facilitates the formation of carbon-carbon bonds, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the synthesis of fluorinated aromatic compounds, which are often used in drug discovery due to their enhanced metabolic stability and bioavailability. Its applications also extend to material science, where it contributes to the creation of organic electronic components and polymers with specific properties.
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