(2-(bis(ethyl-d5)amino)pyrimidin-5-yl)boronic acid

95%

Reagent Code: #56320
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CAS Number 2241877-02-9

science Other reagents with same CAS 2241877-02-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 205.08827778 g/mol
Formula C₈H₄BD₁₀N₃O₂
inventory_2 Storage & Handling
Storage -20℃, sealed and dry

description Product Description

This compound is primarily utilized in the field of pharmaceutical research and development, particularly in the synthesis of complex molecules. It serves as a key intermediate in the creation of targeted therapies, especially in the development of kinase inhibitors. These inhibitors play a crucial role in treating various cancers by blocking specific enzymes that promote tumor growth. Additionally, its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method in organic chemistry to form carbon-carbon bonds. This reaction is essential for constructing biologically active compounds and advanced materials. The deuterium-labeled ethyl groups in the compound enhance its utility in metabolic studies, allowing researchers to track and analyze drug behavior in biological systems with greater precision.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿720,000.00
inventory 5mg
10-20 days ฿269,620.00

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(2-(bis(ethyl-d5)amino)pyrimidin-5-yl)boronic acid
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This compound is primarily utilized in the field of pharmaceutical research and development, particularly in the synthesis of complex molecules. It serves as a key intermediate in the creation of targeted therapies, especially in the development of kinase inhibitors. These inhibitors play a crucial role in treating various cancers by blocking specific enzymes that promote tumor growth. Additionally, its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method

This compound is primarily utilized in the field of pharmaceutical research and development, particularly in the synthesis of complex molecules. It serves as a key intermediate in the creation of targeted therapies, especially in the development of kinase inhibitors. These inhibitors play a crucial role in treating various cancers by blocking specific enzymes that promote tumor growth. Additionally, its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method in organic chemistry to form carbon-carbon bonds. This reaction is essential for constructing biologically active compounds and advanced materials. The deuterium-labeled ethyl groups in the compound enhance its utility in metabolic studies, allowing researchers to track and analyze drug behavior in biological systems with greater precision.

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