[5-(tert-Butyl)-6-methoxy-d12]-pyridine-3-boronic acid

95%

Reagent Code: #92605
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CAS Number 2225179-84-8

science Other reagents with same CAS 2225179-84-8

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Storage -20℃, sealed, dry

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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid functional group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex organic molecules, including pharmaceuticals and agrochemicals. The deuterium-labeled structure (d12) is especially useful in research applications, allowing for precise tracking and analysis of chemical reactions and metabolic pathways in studies involving isotopic labeling. Additionally, the tert-butyl and methoxy groups contribute to the stability and reactivity of the compound, enhancing its performance in synthetic processes.

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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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[5-(tert-Butyl)-6-methoxy-d12]-pyridine-3-boronic acid
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This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid functional group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex organic molecules, including pharmaceuticals and agrochemicals. The deuterium-labeled structure (d12) is especially useful in research applications, allowing for precise tracking and analysis of chemical reactions and metabolic pathways in stu

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic acid functional group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex organic molecules, including pharmaceuticals and agrochemicals. The deuterium-labeled structure (d12) is especially useful in research applications, allowing for precise tracking and analysis of chemical reactions and metabolic pathways in studies involving isotopic labeling. Additionally, the tert-butyl and methoxy groups contribute to the stability and reactivity of the compound, enhancing its performance in synthetic processes.

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