3-(Ethoxycarbonyl)furan-2-boronic acid pinacol ester

95%

Reagent Code: #89997
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CAS Number 2223042-52-0

science Other reagents with same CAS 2223042-52-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 284.11324 g/mol
Formula C₁₃H₂₁BO₆
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 those containing furan rings. Its boronic ester functionality allows for efficient coupling with aryl or vinyl halides, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the synthesis of biologically active compounds and in the preparation of conjugated polymers for electronic applications. The compound's stability and reactivity make it a versatile tool in modern synthetic chemistry.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿24,300.00
inventory 5mg
10-20 days ฿8,280.00

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3-(Ethoxycarbonyl)furan-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 those containing furan rings. Its boronic ester functionality allows for efficient coupling with aryl or vinyl halides, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the synthesis of biologically active

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 those containing furan rings. Its boronic ester functionality allows for efficient coupling with aryl or vinyl halides, making it valuable in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the synthesis of biologically active compounds and in the preparation of conjugated polymers for electronic applications. The compound's stability and reactivity make it a versatile tool in modern synthetic chemistry.

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