5-(3,4-Difluorophenyl)thiazole-4-boronic acid pinacol ester

95%

Reagent Code: #90772
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CAS Number 2223053-44-7

science Other reagents with same CAS 2223053-44-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 341.1811264 g/mol
Formula C₁₅H₁₈BF₂NO₃S
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. 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 bioactive compounds, including potential drug candidates targeting various diseases. Additionally, its difluorophenyl group can enhance the metabolic stability and bioavailability of the resulting molecules, making it a useful building block in medicinal chemistry.

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

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5-(3,4-Difluorophenyl)thiazole-4-boronic acid pinacol ester
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. 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 bioactive compounds, including potential drug candidates targeting various dis

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. 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 bioactive compounds, including potential drug candidates targeting various diseases. Additionally, its difluorophenyl group can enhance the metabolic stability and bioavailability of the resulting molecules, making it a useful building block in medicinal chemistry.

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