(3-Fluoro-5-methylphenyl)boronic acid

98%

Reagent Code: #90178
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CAS Number 850593-06-5

science Other reagents with same CAS 850593-06-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 153.95 g/mol
Formula C₇H₈BFO₂
badge Registry Numbers
MDL Number MFCD07363785
thermostat Physical Properties
Melting Point 216-222°C
Boiling Point 296°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

(3-Fluoro-5-methylphenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the construction of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the synthesis of biologically active compounds, where its boronic acid group facilitates efficient coupling with aryl or vinyl halides. Additionally, it is employed in the development of sensors and probes due to its ability to interact with diols and other functional groups, making it valuable in analytical chemistry and diagnostics. Its fluorine and methyl substituents also enhance its stability and reactivity in various chemical processes.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿711.00
inventory 1g
10-20 days ฿1,728.00

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(3-Fluoro-5-methylphenyl)boronic acid
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(3-Fluoro-5-methylphenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the construction of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the synthesis of biologically active compounds, where its boronic acid group facilitates efficient coupling with aryl or vinyl halides. Additionally,

(3-Fluoro-5-methylphenyl)boronic acid is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is essential for forming carbon-carbon bonds, enabling the construction of complex organic molecules, including pharmaceuticals, agrochemicals, and advanced materials. The compound serves as a key intermediate in the synthesis of biologically active compounds, where its boronic acid group facilitates efficient coupling with aryl or vinyl halides. Additionally, it is employed in the development of sensors and probes due to its ability to interact with diols and other functional groups, making it valuable in analytical chemistry and diagnostics. Its fluorine and methyl substituents also enhance its stability and reactivity in various chemical processes.

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