5-(3-Trifluoromethylphenyl)thiazole-4-boronic acid pinacol ester

95%

Reagent Code: #90789
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CAS Number 2223041-95-8

science Other reagents with same CAS 2223041-95-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 373.1981696 g/mol
Formula C₁₆H₁₉BF₃NO₃S
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronic ester functionality allows for efficient coupling with aryl or vinyl halides, enabling the formation of carbon-carbon bonds. This makes it valuable in the synthesis of biologically active compounds, including potential drug candidates targeting specific diseases. Additionally, it finds use in material science for creating advanced polymers or organic electronic materials due to its ability to introduce specific functional groups into molecular frameworks.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿24,300.00
inventory 5mg
10-20 days ฿8,280.00

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5-(3-Trifluoromethylphenyl)thiazole-4-boronic acid pinacol ester
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronic ester functionality allows for efficient coupling with aryl or vinyl halides, enabling the formation of carbon-carbon bonds. This makes it valuable in the synthesis of biologically active compounds, including potential drug c

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronic ester functionality allows for efficient coupling with aryl or vinyl halides, enabling the formation of carbon-carbon bonds. This makes it valuable in the synthesis of biologically active compounds, including potential drug candidates targeting specific diseases. Additionally, it finds use in material science for creating advanced polymers or organic electronic materials due to its ability to introduce specific functional groups into molecular frameworks.

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