4-Fluoro-3-(trifluoromethyl)benzeneboronic acid

98%

Reagent Code: #90599
label
Alias 4-fluoro-3-(trifluoromethyl)phenylboronic acid
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CAS Number 182344-23-6

science Other reagents with same CAS 182344-23-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 207.92 g/mol
Formula C₇H₅BF₄O₂
badge Registry Numbers
MDL Number MFCD07363787
thermostat Physical Properties
Melting Point 170-174
inventory_2 Storage & Handling
Storage 2~8°C

description Product Description

This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for creating complex organic compounds, including pharmaceuticals and agrochemicals. Its boronic acid group enables it to form stable bonds with various aryl halides, making it valuable in constructing carbon-carbon bonds. Additionally, it is utilized in the development of materials for electronic devices, such as organic light-emitting diodes (OLEDs), due to its ability to modify molecular structures for enhanced performance. Its fluorinated structure also contributes to its stability and reactivity in diverse chemical processes.

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Test Parameter Specification
Purity (HPLC) 98-100%
Infrared Spectrum Conforms to Structure
Appearance White to light yellow powder

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿3,760.00
inventory 1g
10-20 days ฿300.00
inventory 5g
10-20 days ฿760.00

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4-Fluoro-3-(trifluoromethyl)benzeneboronic acid
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This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for creating complex organic compounds, including pharmaceuticals and agrochemicals. Its boronic acid group enables it to form stable bonds with various aryl halides, making it valuable in constructing carbon-carbon bonds. Additionally, it is utilized in the development of materials for electronic devices, such as organic light-emitting diodes (OLEDs), due to its abi

This chemical is widely used in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for creating complex organic compounds, including pharmaceuticals and agrochemicals. Its boronic acid group enables it to form stable bonds with various aryl halides, making it valuable in constructing carbon-carbon bonds. Additionally, it is utilized in the development of materials for electronic devices, such as organic light-emitting diodes (OLEDs), due to its ability to modify molecular structures for enhanced performance. Its fluorinated structure also contributes to its stability and reactivity in diverse chemical processes.

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