1-Methylimidazole-5-boronic Acid Pinacol Ester

≥95%

Reagent Code: #89511
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CAS Number 942070-72-6

science Other reagents with same CAS 942070-72-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 208.07 g/mol
Formula C₁₀H₁₇N₂O₂B
badge Registry Numbers
MDL Number MFCD11846349
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

1-Methylimidazole-5-boronic Acid Pinacol Ester is primarily used in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. This reaction is widely employed in the pharmaceutical industry for the construction of carbon-carbon bonds, enabling the synthesis of complex molecules and drug intermediates. Its boronic ester group acts as a key functional moiety, facilitating the coupling of aryl or vinyl groups with various organic substrates. Additionally, it finds utility in material science for the development of organic electronic materials and polymers. The compound’s stability and reactivity make it a valuable reagent in research and industrial applications for creating advanced chemical structures.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿585.00
inventory 1g
10-20 days ฿1,683.00
inventory 5g
10-20 days ฿7,407.00

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1-Methylimidazole-5-boronic Acid Pinacol Ester
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1-Methylimidazole-5-boronic Acid Pinacol Ester is primarily used in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. This reaction is widely employed in the pharmaceutical industry for the construction of carbon-carbon bonds, enabling the synthesis of complex molecules and drug intermediates. Its boronic ester group acts as a key functional moiety, facilitating the coupling of aryl or vinyl groups with various organic substrates. Additionally, it finds utility

1-Methylimidazole-5-boronic Acid Pinacol Ester is primarily used in organic synthesis, particularly in cross-coupling reactions like the Suzuki-Miyaura reaction. This reaction is widely employed in the pharmaceutical industry for the construction of carbon-carbon bonds, enabling the synthesis of complex molecules and drug intermediates. Its boronic ester group acts as a key functional moiety, facilitating the coupling of aryl or vinyl groups with various organic substrates. Additionally, it finds utility in material science for the development of organic electronic materials and polymers. The compound’s stability and reactivity make it a valuable reagent in research and industrial applications for creating advanced chemical structures.

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