3-(Piperidin-3-yl)-5-cyanophenylboronic acid

95%

Reagent Code: #91849
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CAS Number 2225152-54-3

science Other reagents with same CAS 2225152-54-3

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Weight 230.0707 g/mol
Formula C₁₂H₁₅BN₂O₂
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. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, its piperidine moiety can enhance binding affinity in drug design, making it useful in the development of bioactive compounds targeting neurological and metabolic disorders. The cyano group further contributes to its reactivity, allowing for versatile modifications in medicinal chemistry applications.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿81,900.00

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3-(Piperidin-3-yl)-5-cyanophenylboronic acid
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, its piperidine moiety can enhance binding affinity in drug design, making it useful in the development of bioactive compounds targeting neurological and metabolic disorders. The c

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid group enables the formation of carbon-carbon bonds, making it valuable in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Additionally, its piperidine moiety can enhance binding affinity in drug design, making it useful in the development of bioactive compounds targeting neurological and metabolic disorders. The cyano group further contributes to its reactivity, allowing for versatile modifications in medicinal chemistry applications.

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