5-(Diethylamino)furan-2-boronic acid pinacol ester

95%

Reagent Code: #90826
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CAS Number 2223049-95-2

science Other reagents with same CAS 2223049-95-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 283.17154 g/mol
Formula C₁₄H₂₆BNO₄
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. This reaction is widely employed in the pharmaceutical industry to create complex molecules for drug development. The compound's boronic ester group facilitates the formation of carbon-carbon bonds, making it valuable in constructing biologically active compounds. It is also utilized in material science for the development of organic electronic materials, such as polymers and small molecules with specific optoelectronic properties. Additionally, it finds application in agrochemical research for the synthesis of novel pesticides and herbicides. Its stability and reactivity make it a versatile reagent in various fields of chemical research.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿15,552.00
inventory 100mg
10-20 days ฿46,602.00

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5-(Diethylamino)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. This reaction is widely employed in the pharmaceutical industry to create complex molecules for drug development. The compound's boronic ester group facilitates the formation of carbon-carbon bonds, making it valuable in constructing biologically active compounds. It is also utilized in material science for the development of organic electronic materials, such as polymers and small molecules with spe

Used as a key intermediate in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. This reaction is widely employed in the pharmaceutical industry to create complex molecules for drug development. The compound's boronic ester group facilitates the formation of carbon-carbon bonds, making it valuable in constructing biologically active compounds. It is also utilized in material science for the development of organic electronic materials, such as polymers and small molecules with specific optoelectronic properties. Additionally, it finds application in agrochemical research for the synthesis of novel pesticides and herbicides. Its stability and reactivity make it a versatile reagent in various fields of chemical research.

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