(4-(Diethylcarbamoyl)-3-fluorophenyl)boronic acid

98%

Reagent Code: #90528
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CAS Number 874289-14-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 239.05 g/mol
Formula C₁₁H₁₅BFNO₃
badge Registry Numbers
MDL Number MFCD08436057
thermostat Physical Properties
Melting Point 158-160°C
Boiling Point 433.3°C
inventory_2 Storage & Handling
Density 1.21g/mL
Storage  2-8°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group facilitates the coupling with aryl or vinyl halides, making it valuable in pharmaceutical and material science research. Additionally, the presence of the diethylcarbamoyl and fluorine groups can enhance its reactivity and selectivity in specific reactions, contributing to the development of novel compounds with potential applications in drug discovery and advanced materials.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days $93.94
inventory 1g
10-20 days $253.16
inventory 5g
10-20 days $884.87
(4-(Diethylcarbamoyl)-3-fluorophenyl)boronic acid
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. Its boronic acid group facilitates the coupling with aryl or vinyl halides, making it valuable in pharmaceutical and material science research. Additionally, the presence of the diethylcarbamoyl and fluorine groups can enhance its reactivity and selectivity in specific reactions, contributing to the development of novel compounds with potential applications in drug discovery and advanced materials.
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