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

95%

Reagent Code: #90786
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CAS Number 1402166-53-3

science Other reagents with same CAS 1402166-53-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 310.23986 g/mol
Formula C₁₄H₁₉BO₃S₂
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 Suzuki-Miyaura coupling. It serves as a key intermediate in the production of conjugated polymers and organic semiconductors, which are essential components in the development of organic light-emitting diodes (OLEDs) and organic photovoltaic (OPV) devices. Its thiophene-based structure contributes to the electronic properties of the resulting materials, enhancing their performance in electronic applications. Additionally, it is employed in the synthesis of complex organic molecules for pharmaceutical research and material science, where precise control over molecular architecture is required.

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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-Thienyl)thiophene-2-boronic acid pinacol ester
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate in the production of conjugated polymers and organic semiconductors, which are essential components in the development of organic light-emitting diodes (OLEDs) and organic photovoltaic (OPV) devices. Its thiophene-based structure contributes to the electronic properties of the resulting materials, enhancing their performance in electronic appl

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. It serves as a key intermediate in the production of conjugated polymers and organic semiconductors, which are essential components in the development of organic light-emitting diodes (OLEDs) and organic photovoltaic (OPV) devices. Its thiophene-based structure contributes to the electronic properties of the resulting materials, enhancing their performance in electronic applications. Additionally, it is employed in the synthesis of complex organic molecules for pharmaceutical research and material science, where precise control over molecular architecture is required.

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