2-Cyano-6-(sec-butyl-d9)-pyridine-4-boronic acid

95%

Reagent Code: #59401
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CAS Number 2225152-69-0

science Other reagents with same CAS 2225152-69-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 213.088876002 g/mol
Formula C₁₀H₄BD₉N₂O₂
inventory_2 Storage & Handling
Storage -20℃, sealed and dry

description Product Description

This chemical is primarily utilized in the field of organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a versatile building block for the introduction of the pyridine moiety into more complex molecules, which is valuable in the development of pharmaceuticals and agrochemicals. The deuterium-labeled sec-butyl group enhances its application in research involving isotopic labeling, aiding in mechanistic studies and metabolic pathway analysis. Additionally, its boronic acid functional group makes it a key intermediate in the synthesis of bioactive compounds and materials with potential applications in drug discovery and material science.

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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-Cyano-6-(sec-butyl-d9)-pyridine-4-boronic acid
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This chemical is primarily utilized in the field of organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a versatile building block for the introduction of the pyridine moiety into more complex molecules, which is valuable in the development of pharmaceuticals and agrochemicals. The deuterium-labeled sec-butyl group enhances its application in research involving isotopic labeling, aiding in mechanistic studies and metabolic pathway analysis. Additi

This chemical is primarily utilized in the field of organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. It serves as a versatile building block for the introduction of the pyridine moiety into more complex molecules, which is valuable in the development of pharmaceuticals and agrochemicals. The deuterium-labeled sec-butyl group enhances its application in research involving isotopic labeling, aiding in mechanistic studies and metabolic pathway analysis. Additionally, its boronic acid functional group makes it a key intermediate in the synthesis of bioactive compounds and materials with potential applications in drug discovery and material science.

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