trans-2-[4-(Trifluoromethyl)phenyl]vinylboronic Acid

≥95%

Reagent Code: #122335
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CAS Number 352525-91-8

science Other reagents with same CAS 352525-91-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.96 g/mol
Formula C₉H₈BF₃O₂
badge Registry Numbers
MDL Number MFCD03427005
thermostat Physical Properties
Melting Point 204-210 °C(lit.)
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. Its trifluoromethylphenyl group enhances reactivity and stability, making it valuable in pharmaceutical research for developing drug candidates. Additionally, it is used in material science to create advanced polymers and functional materials with specific electronic or optical properties. Its boronic acid moiety also allows for applications in sensing and detection technologies, particularly in identifying biological molecules.

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inventory 1g
10-20 days ฿8,856.00

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trans-2-[4-(Trifluoromethyl)phenyl]vinylboronic Acid
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. Its trifluoromethylphenyl group enhances reactivity and stability, making it valuable in pharmaceutical research for developing drug candidates. Additionally, it is used in material science to create advanced polymers and functional materials with specific electr
This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. It serves as a key reagent for forming carbon-carbon bonds, enabling the construction of complex organic molecules. Its trifluoromethylphenyl group enhances reactivity and stability, making it valuable in pharmaceutical research for developing drug candidates. Additionally, it is used in material science to create advanced polymers and functional materials with specific electronic or optical properties. Its boronic acid moiety also allows for applications in sensing and detection technologies, particularly in identifying biological molecules.
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