5-(4-Ethylphenyl)thiophene-2-boronic acid pinacol ester

95%

Reagent Code: #90799
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CAS Number 1402227-36-4

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blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 332.2653 g/mol
Formula C₁₈H₂₅BO₃S
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 the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex organic molecules, especially in the development of pharmaceuticals, agrochemicals, and advanced materials. Its boronic ester group facilitates the formation of carbon-carbon bonds, making it valuable for creating conjugated systems in organic electronics, including OLEDs and organic semiconductors. Additionally, it can be employed in the synthesis of biologically active compounds, aiding in drug discovery and development processes. Its stability and reactivity make it a preferred choice for researchers working on precision chemical transformations.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿8,982.00
inventory 25mg
10-20 days ฿19,800.00

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5-(4-Ethylphenyl)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 the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex organic molecules, especially in the development of pharmaceuticals, agrochemicals, and advanced materials. Its boronic ester group facilitates the formation of carbon-carbon bonds, making it valuable for creating conjugated systems in organic electronics, including OLEDs and organic semiconductors. Additionally, i

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex organic molecules, especially in the development of pharmaceuticals, agrochemicals, and advanced materials. Its boronic ester group facilitates the formation of carbon-carbon bonds, making it valuable for creating conjugated systems in organic electronics, including OLEDs and organic semiconductors. Additionally, it can be employed in the synthesis of biologically active compounds, aiding in drug discovery and development processes. Its stability and reactivity make it a preferred choice for researchers working on precision chemical transformations.

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