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

98%

Reagent Code: #90459
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CAS Number 850568-27-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 259.04 g/mol
Formula C₁₃H₁₁BFNO₃
badge Registry Numbers
MDL Number MFCD06659878
thermostat Physical Properties
Melting Point 234-240°C
inventory_2 Storage & Handling
Density 1.34g/mL
Storage  2-8°C

description Product Description

This compound is primarily utilized in organic synthesis and medicinal chemistry as a key intermediate in the development of pharmaceuticals. Its boronic acid functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to create carbon-carbon bonds in the synthesis of complex organic molecules, including potential drug candidates. Specifically, it can be used to introduce aromatic or heteroaromatic structures into target molecules, which is crucial in designing compounds with desired biological activities. Additionally, its fluorophenyl moiety may contribute to enhancing the metabolic stability and binding affinity of drug molecules, making it relevant in the discovery of new therapeutic agents.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days $645.52
[4-[(4-fluorophenyl)carbamoyl]phenyl]boronic acid
This compound is primarily utilized in organic synthesis and medicinal chemistry as a key intermediate in the development of pharmaceuticals. Its boronic acid functional group makes it valuable in Suzuki-Miyaura cross-coupling reactions, which are widely employed to create carbon-carbon bonds in the synthesis of complex organic molecules, including potential drug candidates. Specifically, it can be used to introduce aromatic or heteroaromatic structures into target molecules, which is crucial in designing compounds with desired biological activities. Additionally, its fluorophenyl moiety may contribute to enhancing the metabolic stability and binding affinity of drug molecules, making it relevant in the discovery of new therapeutic agents.
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