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

95%

Reagent Code: #91034
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CAS Number 2223029-79-4

science Other reagents with same CAS 2223029-79-4

blur_circular Chemical Specifications

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

description Product Description

This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronic ester functional group makes it a valuable reagent for forming carbon-carbon bonds, which is essential in the development of pharmaceuticals, agrochemicals, and advanced materials. The deuterated isobutyl and methyl groups enhance its utility in isotopic labeling studies, aiding in the tracking and analysis of chemical reactions and metabolic pathways. Additionally, its stability and reactivity under mild conditions make it suitable for use in complex molecular constructions, often in the synthesis of heterocyclic compounds, which are crucial in drug discovery and development.

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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-(iso-Butyl)-2-methyl-d12]-imidazole-4-boronic acid pinacol ester
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This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronic ester functional group makes it a valuable reagent for forming carbon-carbon bonds, which is essential in the development of pharmaceuticals, agrochemicals, and advanced materials. The deuterated isobutyl and methyl groups enhance its utility in isotopic labeling studies, aiding in the tracking and analysis of chemical reactions and metabolic pathways. Additionally,

This compound is primarily used in organic synthesis, particularly in cross-coupling reactions such as Suzuki-Miyaura coupling. Its boronic ester functional group makes it a valuable reagent for forming carbon-carbon bonds, which is essential in the development of pharmaceuticals, agrochemicals, and advanced materials. The deuterated isobutyl and methyl groups enhance its utility in isotopic labeling studies, aiding in the tracking and analysis of chemical reactions and metabolic pathways. Additionally, its stability and reactivity under mild conditions make it suitable for use in complex molecular constructions, often in the synthesis of heterocyclic compounds, which are crucial in drug discovery and development.

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