[4-[(3-fluorophenyl)carbamoyl]phenyl]boronic acid

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Reagent Code: #89183
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CAS Number 874288-05-8

science Other reagents with same CAS 874288-05-8

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scatter_plot Molecular Information
Weight 259.04 g/mol
Formula C₁₃H₁₁BFNO₃
badge Registry Numbers
MDL Number MFCD09027204
inventory_2 Storage & Handling
Density 1.34g/mL
Storage  2-8°C

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It acts as a key intermediate in the production of complex organic molecules, especially in the pharmaceutical industry for creating drug candidates. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in constructing bioactive compounds. Additionally, it finds applications in materials science for developing advanced polymers and sensors. Its specific structure, incorporating a fluorophenyl group, enhances its utility in designing molecules with targeted biological activity or specific material properties.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿11,800.00
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[4-[(3-fluorophenyl)carbamoyl]phenyl]boronic acid
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It acts as a key intermediate in the production of complex organic molecules, especially in the pharmaceutical industry for creating drug candidates. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in constructing bioactive compounds. Additionally, it finds applications in materials science for developing advanced polymers and sensors. Its specific str

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It acts as a key intermediate in the production of complex organic molecules, especially in the pharmaceutical industry for creating drug candidates. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in constructing bioactive compounds. Additionally, it finds applications in materials science for developing advanced polymers and sensors. Its specific structure, incorporating a fluorophenyl group, enhances its utility in designing molecules with targeted biological activity or specific material properties.

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