(3-Bromo-6-ethoxy-2-fluorophenyl)boronic acid

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Reagent Code: #113211
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CAS Number 1309980-98-0

science Other reagents with same CAS 1309980-98-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 262.87 g/mol
Formula C₈H₉BBrFO₃
badge Registry Numbers
MDL Number MFCD12026724
thermostat Physical Properties
Boiling Point 367.6±52.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex biaryl compounds. These compounds are valuable in pharmaceutical research for developing new drugs. The boronic acid group facilitates the formation of carbon-carbon bonds, making it essential for constructing molecules with potential therapeutic applications. Its specific substitution pattern (bromo, ethoxy, and fluoro groups) allows for precise control over the reactivity and selectivity in chemical transformations. This compound is also employed in material science for designing organic electronic materials.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿891.00
inventory 250mg
10-20 days ฿1,413.00
inventory 1g
10-20 days ฿4,212.00

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(3-Bromo-6-ethoxy-2-fluorophenyl)boronic acid
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Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex biaryl compounds. These compounds are valuable in pharmaceutical research for developing new drugs. The boronic acid group facilitates the formation of carbon-carbon bonds, making it essential for constructing molecules with potential therapeutic applications. Its specific substitution pattern (bromo, ethoxy, and fluoro groups) allows for precise control over the reactivity and selectivity in chemical tr

Used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, to create complex biaryl compounds. These compounds are valuable in pharmaceutical research for developing new drugs. The boronic acid group facilitates the formation of carbon-carbon bonds, making it essential for constructing molecules with potential therapeutic applications. Its specific substitution pattern (bromo, ethoxy, and fluoro groups) allows for precise control over the reactivity and selectivity in chemical transformations. This compound is also employed in material science for designing organic electronic materials.

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