4-Bromo-2-fluoro-6-methoxyphenylboronic acid

98%

Reagent Code: #90657
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CAS Number 957035-32-4

science Other reagents with same CAS 957035-32-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 248.8421 g/mol
Formula C₇H₇BBrFO₃
badge Registry Numbers
MDL Number MFCD09475882
thermostat Physical Properties
Boiling Point 334.9℃ at 760 mmHg
inventory_2 Storage & Handling
Density 1.68±0.1 g/cm3
Storage 2-8℃

description Product Description

This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate in the production of complex organic molecules, including pharmaceuticals and agrochemicals. Its boronic acid group facilitates the formation of carbon-carbon bonds, making it valuable in the synthesis of biaryl compounds, which are common in drug development. Additionally, its specific substitution pattern (bromo, fluoro, and methoxy groups) allows for selective functionalization, enabling the creation of highly tailored compounds for research and industrial applications.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿495.00
inventory 1g
10-20 days ฿1,098.00
inventory 5g
10-20 days ฿5,463.00

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4-Bromo-2-fluoro-6-methoxyphenylboronic acid
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This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate in the production of complex organic molecules, including pharmaceuticals and agrochemicals. Its boronic acid group facilitates the formation of carbon-carbon bonds, making it valuable in the synthesis of biaryl compounds, which are common in drug development. Additionally, its specific substitution pattern (bromo, fluoro, and methoxy groups)

This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate in the production of complex organic molecules, including pharmaceuticals and agrochemicals. Its boronic acid group facilitates the formation of carbon-carbon bonds, making it valuable in the synthesis of biaryl compounds, which are common in drug development. Additionally, its specific substitution pattern (bromo, fluoro, and methoxy groups) allows for selective functionalization, enabling the creation of highly tailored compounds for research and industrial applications.

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