2,5-Dimethoxy-2,5-dihydrofuran-3-boronic acid pinacol ester

95%

Reagent Code: #89574
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CAS Number 2223003-40-3

science Other reagents with same CAS 2223003-40-3

blur_circular Chemical Specifications

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Weight 274.11842 g/mol
Formula C₁₂H₂₃BO₆
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 versatile building block for introducing functionalized furan rings into more complex molecules. The boronic ester group facilitates the formation of carbon-carbon bonds, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity under mild conditions make it a preferred choice for constructing heterocyclic compounds, which are often key components in drug discovery and development. Additionally, it can be used in the preparation of conjugated polymers for electronic applications, leveraging its ability to integrate into π-conjugated systems.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿9,612.00
inventory 25mg
10-20 days ฿21,600.00

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2,5-Dimethoxy-2,5-dihydrofuran-3-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 versatile building block for introducing functionalized furan rings into more complex molecules. The boronic ester group facilitates the formation of carbon-carbon bonds, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity under mild conditions make it a preferred choice for constructi

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a versatile building block for introducing functionalized furan rings into more complex molecules. The boronic ester group facilitates the formation of carbon-carbon bonds, making it valuable in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Its stability and reactivity under mild conditions make it a preferred choice for constructing heterocyclic compounds, which are often key components in drug discovery and development. Additionally, it can be used in the preparation of conjugated polymers for electronic applications, leveraging its ability to integrate into π-conjugated systems.

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