3,5-Bis(piperidino)phenylboronic acid

95%

Reagent Code: #89924
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CAS Number 2225177-64-8

science Other reagents with same CAS 2225177-64-8

blur_circular Chemical Specifications

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Weight 288.1929 g/mol
Formula C₁₆H₂₅BN₂O₂
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

Used in organic synthesis as a key intermediate for the preparation of complex molecules, particularly in the development of pharmaceuticals and bioactive compounds. Its boronic acid group facilitates Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. This is crucial in creating diverse organic structures, including drug candidates and materials with specific functionalities. Additionally, it serves as a ligand in catalysis, enhancing the efficiency of transition metal-catalyzed reactions. Its piperidino groups contribute to solubility and stability, making it suitable for use in various reaction conditions.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿10,080.00
inventory 25mg
10-20 days ฿29,304.00
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3,5-Bis(piperidino)phenylboronic acid
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Used in organic synthesis as a key intermediate for the preparation of complex molecules, particularly in the development of pharmaceuticals and bioactive compounds. Its boronic acid group facilitates Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. This is crucial in creating diverse organic structures, including drug candidates and materials with specific functionalities. Additionally, it serves as a ligand in catalysis, enhancing the efficiency of transition meta

Used in organic synthesis as a key intermediate for the preparation of complex molecules, particularly in the development of pharmaceuticals and bioactive compounds. Its boronic acid group facilitates Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. This is crucial in creating diverse organic structures, including drug candidates and materials with specific functionalities. Additionally, it serves as a ligand in catalysis, enhancing the efficiency of transition metal-catalyzed reactions. Its piperidino groups contribute to solubility and stability, making it suitable for use in various reaction conditions.

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