(2,3-Difluoro-4-isopropoxyphenyl)boronic acid

98%

Reagent Code: #167195
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CAS Number 1154762-01-2

science Other reagents with same CAS 1154762-01-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.9896 g/mol
Formula C₉H₁₁BF₂O₃
badge Registry Numbers
MDL Number MFCD19237183
thermostat Physical Properties
Boiling Point 321.1±52.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.25±0.1 g/cm3(Predicted)
Storage 2-8°C, 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 fluorinated compounds. The presence of fluorine atoms and an isopropoxy group enhances electronic and metabolic stability, which is beneficial in drug design. Commonly applied in the preparation of bioactive molecules and functional materials requiring tailored aromatic structures.

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inventory 1g
10-20 days ฿11,000.00

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(2,3-Difluoro-4-isopropoxyphenyl)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 fluorinated compounds. The presence of fluorine atoms and an isopropoxy group enhances electronic and metabolic stability, which is beneficial in drug design. Commonly applied in the preparation of bioactive molecules and

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 fluorinated compounds. The presence of fluorine atoms and an isopropoxy group enhances electronic and metabolic stability, which is beneficial in drug design. Commonly applied in the preparation of bioactive molecules and functional materials requiring tailored aromatic structures.

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