4-(3-Thienyl)furan-2-boronic acid pinacol ester

95%

Reagent Code: #90395
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CAS Number 2223011-21-8

science Other reagents with same CAS 2223011-21-8

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Weight 294.17426 g/mol
Formula C₁₄H₁₉BO₄S
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic ester group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex organic molecules. It is often employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its thienyl and furan moieties contribute to its use in the development of conjugated polymers and organic electronic materials, which are essential in applications like organic light-emitting diodes (OLEDs) and organic photovoltaics. Its stability and reactivity make it a versatile reagent in both academic research and industrial processes.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿29,304.00
inventory 5mg
10-20 days ฿10,080.00

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4-(3-Thienyl)furan-2-boronic acid pinacol ester
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This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic ester group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex organic molecules. It is often employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its thienyl and furan moieties contribute to its use in the development of conjugated polymers and organic electronic mater

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic ester group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex organic molecules. It is often employed in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Additionally, its thienyl and furan moieties contribute to its use in the development of conjugated polymers and organic electronic materials, which are essential in applications like organic light-emitting diodes (OLEDs) and organic photovoltaics. Its stability and reactivity make it a versatile reagent in both academic research and industrial processes.

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