2-Methyl-5-(sec-butyl)furan-3-boronic acid pinacol ester

95%

Reagent Code: #89757
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CAS Number 2223003-30-1

science Other reagents with same CAS 2223003-30-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 282.18348 g/mol
Formula C₁₅H₂₇BO₄
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions like Suzuki-Miyaura coupling. It serves as a key intermediate for constructing complex organic molecules, especially in pharmaceuticals and agrochemicals. Its boronic ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of aryl and heteroaryl compounds. Additionally, it is employed in material science for developing advanced polymers and organic electronic materials. Its stability and reactivity make it a valuable tool in research and industrial applications for creating tailored chemical structures.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿96,000.00
inventory 100mg
10-20 days ฿285,000.00

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2-Methyl-5-(sec-butyl)furan-3-boronic acid pinacol ester
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This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions like Suzuki-Miyaura coupling. It serves as a key intermediate for constructing complex organic molecules, especially in pharmaceuticals and agrochemicals. Its boronic ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of aryl and heteroaryl compounds. Additionally, it is employed in material science for developing advanced polymers and organic electronic materials. Its stabilit

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions like Suzuki-Miyaura coupling. It serves as a key intermediate for constructing complex organic molecules, especially in pharmaceuticals and agrochemicals. Its boronic ester group facilitates the formation of carbon-carbon bonds, enabling the synthesis of aryl and heteroaryl compounds. Additionally, it is employed in material science for developing advanced polymers and organic electronic materials. Its stability and reactivity make it a valuable tool in research and industrial applications for creating tailored chemical structures.

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