4-(4-Fluorophenyl)furan-2-boronic acid

95%

Reagent Code: #90428
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CAS Number 2096331-23-4

science Other reagents with same CAS 2096331-23-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 205.9781232 g/mol
Formula C₁₀H₈BFO₃
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

Used primarily in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate for creating complex organic molecules. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development of fluorescent probes and sensors due to its ability to interact with specific biological targets. The fluorophenyl group enhances its stability and reactivity, making it suitable for applications in medicinal chemistry and drug discovery.

Available Sizes & Pricing

Size Availability Unit Price Quantity
5mg
10-20 days ฿8,280.00
25mg
10-20 days ฿24,300.00
4-(4-Fluorophenyl)furan-2-boronic acid
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Used primarily in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate for creating complex organic molecules. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development of fluorescent probes and sensors due to its ability to interact with specific biological targets. The fluorophenyl gro

Used primarily in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, this compound serves as a key intermediate for creating complex organic molecules. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the production of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the development of fluorescent probes and sensors due to its ability to interact with specific biological targets. The fluorophenyl group enhances its stability and reactivity, making it suitable for applications in medicinal chemistry and drug discovery.

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