(4-Fluorobenzo[d][1,3]dioxol-5-yl)boronic acid

98%

Reagent Code: #168311
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CAS Number 943830-75-9

science Other reagents with same CAS 943830-75-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 183.93 g/mol
Formula C₇H₆BFO₄
badge Registry Numbers
MDL Number MFCD12025969
thermostat Physical Properties
Boiling Point 339.7±52.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.51±0.1 g/cm3(Predicted)
Storage 2-8°C, Sealed, Inert Gas

description Product Description

Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the development of complex molecules for drug discovery. The fluorinated benzodioxole structure enhances metabolic stability and binding affinity in bioactive compounds, often exploited in medicinal chemistry for designing CNS agents, antiviral drugs, and enzyme inhibitors. Also applied in materials science for creating functionalized organic semiconductors and fluorescent probes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿13,470.00
inventory 250mg
10-20 days ฿25,270.00

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(4-Fluorobenzo[d][1,3]dioxol-5-yl)boronic acid
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Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the development of complex molecules for drug discovery. The fluorinated benzodioxole structure enhances metabolic stability and binding affinity in bioactive compounds, often exploited in medicinal chemistry for designing CNS agents, antiviral dru

Used in organic synthesis as a building block for pharmaceuticals and agrochemicals, particularly in Suzuki-Miyaura cross-coupling reactions to form carbon-carbon bonds. Its boronic acid group enables efficient coupling with aryl halides, making it valuable in the development of complex molecules for drug discovery. The fluorinated benzodioxole structure enhances metabolic stability and binding affinity in bioactive compounds, often exploited in medicinal chemistry for designing CNS agents, antiviral drugs, and enzyme inhibitors. Also applied in materials science for creating functionalized organic semiconductors and fluorescent probes.

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