3-FLUORO-5-(N-PROPYLCARBAMOYL)BENZENEBORONIC ACID

98%

Reagent Code: #90167
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CAS Number 874219-37-1
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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 225.0245 g/mol
Formula C₁₀H₁₃BFNO₃
badge Registry Numbers
MDL Number MFCD08235054
thermostat Physical Properties
Melting Point 95-97 °C
inventory_2 Storage & Handling
Density 1.23 g/cm3
Storage 2-8°C

description Product Description

Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of various pharmaceuticals and bioactive molecules. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, a widely utilized method for forming carbon-carbon bonds. This makes it valuable in the development of complex organic compounds, including potential drug candidates. Additionally, its fluorine substitution enhances its metabolic stability and binding affinity, making it suitable for use in medicinal chemistry research. The compound is also employed in the synthesis of materials for organic electronics due to its ability to modify electronic properties.

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Size Availability Unit Price Quantity
inventory 1mg
10-20 days ฿4,950.00
inventory 5g
10-20 days ฿15,012.00

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3-FLUORO-5-(N-PROPYLCARBAMOYL)BENZENEBORONIC ACID
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Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of various pharmaceuticals and bioactive molecules. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, a widely utilized method for forming carbon-carbon bonds. This makes it valuable in the development of complex organic compounds, including potential drug candidates. Additionally, its fluorine substitution enhances its metabolic stability and binding affinity, mak

Used primarily in organic synthesis, this compound serves as a key intermediate in the preparation of various pharmaceuticals and bioactive molecules. Its boronic acid group enables it to participate in Suzuki-Miyaura cross-coupling reactions, a widely utilized method for forming carbon-carbon bonds. This makes it valuable in the development of complex organic compounds, including potential drug candidates. Additionally, its fluorine substitution enhances its metabolic stability and binding affinity, making it suitable for use in medicinal chemistry research. The compound is also employed in the synthesis of materials for organic electronics due to its ability to modify electronic properties.

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