(2-((tert-Butoxycarbonyl)amino)pyrimidin-5-yl)boronic acid

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Reagent Code: #91054
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CAS Number 883231-25-2

science Other reagents with same CAS 883231-25-2

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Weight 239.04 g/mol
Formula C₉H₁₄BN₃O₄
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical research and development. Its boronic acid group enables efficient coupling with aryl or vinyl halides, facilitating the creation of carbon-carbon bonds. This makes it valuable in the synthesis of bioactive compounds, including potential drug candidates. Additionally, it is employed in the preparation of pyrimidine derivatives, which are essential in medicinal chemistry for designing molecules with therapeutic properties. Its tert-butoxycarbonyl (Boc) protecting group ensures stability during synthetic processes, allowing for selective deprotection when needed.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,061.00
inventory 1g
10-20 days ฿3,996.00

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(2-((tert-Butoxycarbonyl)amino)pyrimidin-5-yl)boronic acid
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This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical research and development. Its boronic acid group enables efficient coupling with aryl or vinyl halides, facilitating the creation of carbon-carbon bonds. This makes it valuable in the synthesis of bioactive compounds, including potential drug candidates. Additionally, it is emplo

This chemical is primarily used in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a key intermediate for constructing complex molecules, especially in pharmaceutical research and development. Its boronic acid group enables efficient coupling with aryl or vinyl halides, facilitating the creation of carbon-carbon bonds. This makes it valuable in the synthesis of bioactive compounds, including potential drug candidates. Additionally, it is employed in the preparation of pyrimidine derivatives, which are essential in medicinal chemistry for designing molecules with therapeutic properties. Its tert-butoxycarbonyl (Boc) protecting group ensures stability during synthetic processes, allowing for selective deprotection when needed.

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