(3-Bromo-2-fluorophenyl)boronic acid

95%

Reagent Code: #90227
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CAS Number 352535-97-8

science Other reagents with same CAS 352535-97-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 218.82 g/mol
Formula C₆H₅BBrFO₂
thermostat Physical Properties
Melting Point 225-227°C
Boiling Point 326.6°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

(3-Bromo-2-fluorophenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the synthesis of complex organic molecules due to its ability to react with various aryl halides in the presence of a palladium catalyst. Additionally, it is utilized in the development of bioactive compounds and in research focused on creating new drug candidates. Its unique structure, combining bromo and fluoro substituents, allows for selective reactivity, making it a versatile tool in medicinal chemistry and material science.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿423.00
inventory 5g
10-20 days ฿1,908.00
inventory 25g
10-20 days ฿8,352.00

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(3-Bromo-2-fluorophenyl)boronic acid
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(3-Bromo-2-fluorophenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the synthesis of complex organic molecules due to its ability to react with various aryl halides in the presence of a palladium catalyst. Additionally, it is utilized in the dev

(3-Bromo-2-fluorophenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the synthesis of complex organic molecules due to its ability to react with various aryl halides in the presence of a palladium catalyst. Additionally, it is utilized in the development of bioactive compounds and in research focused on creating new drug candidates. Its unique structure, combining bromo and fluoro substituents, allows for selective reactivity, making it a versatile tool in medicinal chemistry and material science.

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