4-(4-Methylpiperidin-1-yl)furan-2-boronic acid

95%

Reagent Code: #46275
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CAS Number 2225174-13-8

science Other reagents with same CAS 2225174-13-8

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Weight 209.04994 g/mol
Formula C₁₀H₁₆BNO₃
inventory_2 Storage & Handling
Storage -20℃

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a boronic acid reagent to form carbon-carbon bonds. Its structure, featuring a furan ring and a piperidine moiety, makes it valuable in the construction of complex molecules, including pharmaceuticals and agrochemicals. The compound’s boronic acid group is key for its reactivity, enabling the formation of biaryl or heteroaryl structures, which are common in active drug ingredients. Additionally, it may be employed in the development of materials science applications, such as organic electronic materials, due to its potential for creating conjugated systems.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿19,890.00
inventory 5mg
10-20 days ฿5,094.00

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4-(4-Methylpiperidin-1-yl)furan-2-boronic acid
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a boronic acid reagent to form carbon-carbon bonds. Its structure, featuring a furan ring and a piperidine moiety, makes it valuable in the construction of complex molecules, including pharmaceuticals and agrochemicals. The compound’s boronic acid group is key for its reactivity, enabling the formation of biaryl or heteroaryl structures, which are common

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it acts as a boronic acid reagent to form carbon-carbon bonds. Its structure, featuring a furan ring and a piperidine moiety, makes it valuable in the construction of complex molecules, including pharmaceuticals and agrochemicals. The compound’s boronic acid group is key for its reactivity, enabling the formation of biaryl or heteroaryl structures, which are common in active drug ingredients. Additionally, it may be employed in the development of materials science applications, such as organic electronic materials, due to its potential for creating conjugated systems.

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