3-(METHOXYCARBONYL)FURAN-2-BORONIC ACID PINACOL ESTER

95%

Reagent Code: #89999
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CAS Number 2223051-20-3

science Other reagents with same CAS 2223051-20-3

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Weight 270.08666 g/mol
Formula C₁₂H₁₉BO₆
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic ester group facilitates the formation of carbon-carbon bonds, enabling the construction of complex molecular structures. This compound is also valuable in the development of furan-based compounds, which are utilized in drug discovery and material science due to their versatile reactivity and potential biological activity. Additionally, it serves as a building block in the synthesis of organic electronic materials, contributing to the advancement of optoelectronic devices.

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

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3-(METHOXYCARBONYL)FURAN-2-BORONIC ACID PINACOL ESTER
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Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic ester group facilitates the formation of carbon-carbon bonds, enabling the construction of complex molecular structures. This compound is also valuable in the development of furan-based compounds, which are utilized in drug discovery and material science due to their versatile reactivity

Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, which are widely employed in the production of pharmaceuticals, agrochemicals, and advanced materials. Its boronic ester group facilitates the formation of carbon-carbon bonds, enabling the construction of complex molecular structures. This compound is also valuable in the development of furan-based compounds, which are utilized in drug discovery and material science due to their versatile reactivity and potential biological activity. Additionally, it serves as a building block in the synthesis of organic electronic materials, contributing to the advancement of optoelectronic devices.

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