5-(4-Fluorophenyl)thiazole-4-boronic acid pinacol ester

95%

Reagent Code: #90800
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CAS Number 2223031-99-8

science Other reagents with same CAS 2223031-99-8

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Weight 323.1906632 g/mol
Formula C₁₅H₁₉BFNO₃S
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 the construction of complex molecules, especially in the development of pharmaceuticals and agrochemicals. The boronic ester group facilitates the formation of carbon-carbon bonds, enabling the attachment of aromatic or heteroaromatic systems. Its fluorophenyl moiety often contributes to the biological activity of the final compounds, making it valuable in drug discovery for targeting specific receptors or enzymes. Additionally, it is used in material science for the synthesis of organic electronic materials, where its structural properties can influence conductivity or optical characteristics.

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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-(4-Fluorophenyl)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 the construction of complex molecules, especially in the development of pharmaceuticals and agrochemicals. The boronic ester group facilitates the formation of carbon-carbon bonds, enabling the attachment of aromatic or heteroaromatic systems. Its fluorophenyl moiety often contributes to the biological activity of the final compounds, making it valuable in

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for the construction of complex molecules, especially in the development of pharmaceuticals and agrochemicals. The boronic ester group facilitates the formation of carbon-carbon bonds, enabling the attachment of aromatic or heteroaromatic systems. Its fluorophenyl moiety often contributes to the biological activity of the final compounds, making it valuable in drug discovery for targeting specific receptors or enzymes. Additionally, it is used in material science for the synthesis of organic electronic materials, where its structural properties can influence conductivity or optical characteristics.

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