(4-Carbamoyl-2-fluorophenyl)boronic acid

98%

Reagent Code: #90617
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CAS Number 874289-22-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 182.94 g/mol
Formula C₇H₇BFNO₃
badge Registry Numbers
MDL Number MFCD09800867
thermostat Physical Properties
Boiling Point 359.8°C
inventory_2 Storage & Handling
Density 1.41g/mL
Storage  2-8°C

description Product Description

(4-Carbamoyl-2-fluorophenyl)boronic acid is primarily used in organic synthesis, particularly in cross-coupling reactions like Suzuki-Miyaura coupling. This reaction is widely employed to form carbon-carbon bonds, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, enabling the formation of complex organic molecules. Additionally, it is utilized in the development of bioactive compounds and drug candidates due to its ability to interact with biological targets. Its fluorophenyl moiety further enhances its utility in creating compounds with specific electronic and steric properties.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿3,380.00
inventory 1g
10-20 days ฿10,000.00
(4-Carbamoyl-2-fluorophenyl)boronic acid
(4-Carbamoyl-2-fluorophenyl)boronic acid is primarily used in organic synthesis, particularly in cross-coupling reactions like Suzuki-Miyaura coupling. This reaction is widely employed to form carbon-carbon bonds, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its boronic acid group acts as a key intermediate, enabling the formation of complex organic molecules. Additionally, it is utilized in the development of bioactive compounds and drug candidates due to its ability to interact with biological targets. Its fluorophenyl moiety further enhances its utility in creating compounds with specific electronic and steric properties.
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