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

95%

Reagent Code: #89994
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CAS Number 2223029-74-9

science Other reagents with same CAS 2223029-74-9

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Weight 254.08726 g/mol
Formula C₁₂H₁₉BO₅
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

This chemical is widely used 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 pharmaceutical and agrochemical industries. Its boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the creation of carbon-carbon bonds. This makes it valuable in the development of drugs, bioactive compounds, and advanced materials. Additionally, it is utilized in the synthesis of heterocyclic compounds, which are essential in medicinal chemistry for designing molecules with specific biological activities. Its stability and reactivity under mild conditions make it a preferred choice for researchers in synthetic chemistry.

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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-(Acetyl)furan-2-boronic acid pinacol ester
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This chemical is widely used 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 pharmaceutical and agrochemical industries. Its boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the creation of carbon-carbon bonds. This makes it valuable in the development of drugs, bioactive compounds, and advanced materials. Additionally, it

This chemical is widely used 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 pharmaceutical and agrochemical industries. Its boronic ester group enables efficient coupling with aryl or vinyl halides, facilitating the creation of carbon-carbon bonds. This makes it valuable in the development of drugs, bioactive compounds, and advanced materials. Additionally, it is utilized in the synthesis of heterocyclic compounds, which are essential in medicinal chemistry for designing molecules with specific biological activities. Its stability and reactivity under mild conditions make it a preferred choice for researchers in synthetic chemistry.

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