[1-(sec-Butyl)-2-methyl-d12]-imidazole-4-boronic acid pinacol ester

95%

Reagent Code: #91036
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CAS Number 2223006-39-9

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blur_circular Chemical Specifications

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Weight 294.260721336 g/mol
Formula C₁₄H₁₅BD₁₂N₂O₃
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic ester group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex organic molecules, including pharmaceuticals and agrochemicals. The deuterium labeling (d12) enhances its utility in research involving isotopic labeling, aiding in mechanistic studies and metabolic pathway analysis. Its stability and reactivity make it a preferred choice in medicinal chemistry for developing drug candidates with improved pharmacokinetic properties.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿269,660.00
inventory 25mg
10-20 days ฿699,980.00

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[1-(sec-Butyl)-2-methyl-d12]-imidazole-4-boronic acid pinacol ester
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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 ester group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex organic molecules, including pharmaceuticals and agrochemicals. The deuterium labeling (d12) enhances its utility in research involving isotopic labeling, aiding in mechanistic studies and metabolic pathway analysis. Its stability and reactivity make it

This compound is primarily utilized in organic synthesis, particularly in cross-coupling reactions such as the Suzuki-Miyaura reaction. Its boronic ester group enables the formation of carbon-carbon bonds, making it valuable in the construction of complex organic molecules, including pharmaceuticals and agrochemicals. The deuterium labeling (d12) enhances its utility in research involving isotopic labeling, aiding in mechanistic studies and metabolic pathway analysis. Its stability and reactivity make it a preferred choice in medicinal chemistry for developing drug candidates with improved pharmacokinetic properties.

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