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

95%

Reagent Code: #90760
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CAS Number 2223031-90-9

science Other reagents with same CAS 2223031-90-9

blur_circular Chemical Specifications

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Weight 294.17426 g/mol
Formula C₁₄H₁₉BO₄S
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 building block for the construction of complex organic molecules, especially in the development of pharmaceuticals and agrochemicals. The furyl and thiophene moieties in its structure make it valuable for creating conjugated systems, which are essential in materials science for applications like organic semiconductors and light-emitting diodes (OLEDs). Additionally, its boronic ester group enhances its stability and reactivity, making it suitable for use in various catalytic processes.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿40,200.00
inventory 100mg
10-20 days ฿128,000.00

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5-(2-Furyl)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 building block for the construction of complex organic molecules, especially in the development of pharmaceuticals and agrochemicals. The furyl and thiophene moieties in its structure make it valuable for creating conjugated systems, which are essential in materials science for applications like organic semiconductors and light-emitting diodes (OLEDs).

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key building block for the construction of complex organic molecules, especially in the development of pharmaceuticals and agrochemicals. The furyl and thiophene moieties in its structure make it valuable for creating conjugated systems, which are essential in materials science for applications like organic semiconductors and light-emitting diodes (OLEDs). Additionally, its boronic ester group enhances its stability and reactivity, making it suitable for use in various catalytic processes.

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