2-(sec-Butyl-d9)-6-fluoropyridine-4-boronic acid

95%

Reagent Code: #62742
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CAS Number 2225152-00-9

science Other reagents with same CAS 2225152-00-9

blur_circular Chemical Specifications

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Weight 206.069879202 g/mol
Formula C₉H₄BD₉FNO₂
inventory_2 Storage & Handling
Storage -20℃, sealed and dry

description Product Description

This compound is primarily used in the pharmaceutical and chemical research industries as a building block in the synthesis of more complex molecules. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This is particularly useful in creating novel drug candidates and organic materials. The deuterium-labeled sec-butyl group enhances its utility in metabolic studies and tracing mechanisms in drug development, providing insights into the behavior of compounds in biological systems. Additionally, the fluorine atom can influence the pharmacokinetic properties of the resulting molecules, making it a key component in the design of bioactive compounds.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿269,620.00
inventory 25mg
10-20 days ฿720,000.00
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2-(sec-Butyl-d9)-6-fluoropyridine-4-boronic acid
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This compound is primarily used in the pharmaceutical and chemical research industries as a building block in the synthesis of more complex molecules. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This is particularly useful in creating novel drug candidates and organic materials. The deuterium-labeled sec-butyl group enhances its utility in metabolic studies and tracing mechanisms in drug development, providing

This compound is primarily used in the pharmaceutical and chemical research industries as a building block in the synthesis of more complex molecules. Its boronic acid group makes it valuable in Suzuki-Miyaura cross-coupling reactions, a widely used method for forming carbon-carbon bonds. This is particularly useful in creating novel drug candidates and organic materials. The deuterium-labeled sec-butyl group enhances its utility in metabolic studies and tracing mechanisms in drug development, providing insights into the behavior of compounds in biological systems. Additionally, the fluorine atom can influence the pharmacokinetic properties of the resulting molecules, making it a key component in the design of bioactive compounds.

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