4-Chloro-2-(4-hydroxypiperidino)pyrimidine-5-boronic acid

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Reagent Code: #92083
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CAS Number 2225172-86-9

science Other reagents with same CAS 2225172-86-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 257.48182 g/mol
Formula C₉H₁₃BClN₃O₃
inventory_2 Storage & Handling
Storage -20℃, sealed and dry

description Product Description

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it serves as a boronic acid derivative. Its structure allows it to act as a key intermediate in the preparation of complex organic molecules, including pharmaceuticals and agrochemicals. The presence of the boronic acid group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. Additionally, the piperidine moiety in its structure can contribute to the biological activity of the final compounds, making it valuable in drug discovery and development processes. Its applications are often focused on creating compounds with potential therapeutic or agricultural benefits.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿8,982.00
inventory 25mg
10-20 days ฿29,700.00
inventory 100mg
10-20 days ฿82,800.00

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4-Chloro-2-(4-hydroxypiperidino)pyrimidine-5-boronic acid
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This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it serves as a boronic acid derivative. Its structure allows it to act as a key intermediate in the preparation of complex organic molecules, including pharmaceuticals and agrochemicals. The presence of the boronic acid group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. Additionally, the piperidine moiety

This chemical is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction, where it serves as a boronic acid derivative. Its structure allows it to act as a key intermediate in the preparation of complex organic molecules, including pharmaceuticals and agrochemicals. The presence of the boronic acid group enables efficient coupling with aryl or vinyl halides, facilitating the formation of carbon-carbon bonds. Additionally, the piperidine moiety in its structure can contribute to the biological activity of the final compounds, making it valuable in drug discovery and development processes. Its applications are often focused on creating compounds with potential therapeutic or agricultural benefits.

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