2-(3-Trifluoromethylphenyl)pyridine-4-boronic acid

95%

Reagent Code: #91488
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CAS Number 2225180-64-1

science Other reagents with same CAS 2225180-64-1

blur_circular Chemical Specifications

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Weight 267.0115696 g/mol
Formula C₁₂H₉BF₃NO₂
inventory_2 Storage & Handling
Storage -20℃, sealed and dry

description Product Description

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for the preparation of more complex organic compounds, especially in the pharmaceutical and agrochemical industries. The trifluoromethyl group enhances the stability and reactivity of the compound, making it valuable in the development of active pharmaceutical ingredients (APIs) and other biologically active molecules. Additionally, its boronic acid functional group allows for efficient coupling with aryl halides, enabling the creation of diverse biaryl structures. This compound is also utilized in material science for the synthesis of advanced materials, including organic electronics and liquid crystals.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿82,800.00
inventory 5mg
10-20 days ฿8,982.00
inventory 25mg
10-20 days ฿29,700.00

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2-(3-Trifluoromethylphenyl)pyridine-4-boronic acid
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This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for the preparation of more complex organic compounds, especially in the pharmaceutical and agrochemical industries. The trifluoromethyl group enhances the stability and reactivity of the compound, making it valuable in the development of active pharmaceutical ingredients (APIs) and other biologically active molecules. Additionally, its boroni

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for the preparation of more complex organic compounds, especially in the pharmaceutical and agrochemical industries. The trifluoromethyl group enhances the stability and reactivity of the compound, making it valuable in the development of active pharmaceutical ingredients (APIs) and other biologically active molecules. Additionally, its boronic acid functional group allows for efficient coupling with aryl halides, enabling the creation of diverse biaryl structures. This compound is also utilized in material science for the synthesis of advanced materials, including organic electronics and liquid crystals.

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