5-(3-Furyl)thiophene-2-boronic acid pinacol ester

95%

Reagent Code: #90778
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CAS Number 2223011-14-9

science Other reagents with same CAS 2223011-14-9

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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 used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key building block for constructing complex organic molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronic ester group facilitates the formation of carbon-carbon bonds, making it valuable in creating heterocyclic compounds. Additionally, it is employed in material science for synthesizing conjugated polymers, which are essential in organic electronics like OLEDs and solar cells. Its furyl and thiophene moieties contribute to the electronic properties of the resulting materials, enhancing their performance in optoelectronic applications.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿28,080.00
inventory 100mg
10-20 days ฿87,120.00

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5-(3-Furyl)thiophene-2-boronic acid pinacol ester
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This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key building block for constructing complex organic molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronic ester group facilitates the formation of carbon-carbon bonds, making it valuable in creating heterocyclic compounds. Additionally, it is employed in material science for synthesizing conjugated polymers, which are essential

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key building block for constructing complex organic molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronic ester group facilitates the formation of carbon-carbon bonds, making it valuable in creating heterocyclic compounds. Additionally, it is employed in material science for synthesizing conjugated polymers, which are essential in organic electronics like OLEDs and solar cells. Its furyl and thiophene moieties contribute to the electronic properties of the resulting materials, enhancing their performance in optoelectronic applications.

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