[2-(tert-Butyl)-3-methyl-d12]-pyridine-4-boronic acid

95%

Reagent Code: #92578
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CAS Number 2225179-78-0

science Other reagents with same CAS 2225179-78-0

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inventory_2 Storage & Handling
Storage -20℃, sealed and dry

description Product Description

This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. It serves as a valuable boronic acid reagent for introducing the [2-(tert-butyl)-3-methyl-d12]-pyridine moiety into various organic molecules. Its deuterated structure makes it useful in isotopic labeling studies, aiding in the tracking and analysis of chemical reactions and metabolic pathways in pharmaceutical research. Additionally, it is employed in the development of advanced materials and ligands for catalysis, where its steric and electronic properties can influence reaction outcomes.

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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-(tert-Butyl)-3-methyl-d12]-pyridine-4-boronic acid
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This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. It serves as a valuable boronic acid reagent for introducing the [2-(tert-butyl)-3-methyl-d12]-pyridine moiety into various organic molecules. Its deuterated structure makes it useful in isotopic labeling studies, aiding in the tracking and analysis of chemical reactions and metabolic pathways in pharmaceutical research. Additionally, it is employed in the development of advanc

This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura reactions. It serves as a valuable boronic acid reagent for introducing the [2-(tert-butyl)-3-methyl-d12]-pyridine moiety into various organic molecules. Its deuterated structure makes it useful in isotopic labeling studies, aiding in the tracking and analysis of chemical reactions and metabolic pathways in pharmaceutical research. Additionally, it is employed in the development of advanced materials and ligands for catalysis, where its steric and electronic properties can influence reaction outcomes.

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