4-(Imidazol-1-yl)thiophene-2-boronic acid pinacol ester

95%

Reagent Code: #90493
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CAS Number 2223032-27-5

science Other reagents with same CAS 2223032-27-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 294.17756 g/mol
Formula C₁₃H₁₉BN₂O₃S
inventory_2 Storage & Handling
Storage -20°C, sealed, dry

description Product Description

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronic ester group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Additionally, it is employed in the synthesis of thiophene-based materials, which are essential in organic electronics, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Its imidazole moiety further enhances its utility in designing biologically active compounds, including potential drug candidates targeting various diseases.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿15,552.00
inventory 100mg
10-20 days ฿46,602.00

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4-(Imidazol-1-yl)thiophene-2-boronic acid pinacol ester
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This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronic ester group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Additionally, it is employed in the synthesis of thiophene-based materials, which are essential in organic electronics, such as organic l

This compound is primarily utilized in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions. It serves as a key intermediate for constructing complex molecules, especially in the development of pharmaceuticals and agrochemicals. Its boronic ester group enables efficient coupling with aryl halides, facilitating the formation of carbon-carbon bonds. Additionally, it is employed in the synthesis of thiophene-based materials, which are essential in organic electronics, such as organic light-emitting diodes (OLEDs) and organic photovoltaics (OPVs). Its imidazole moiety further enhances its utility in designing biologically active compounds, including potential drug candidates targeting various diseases.

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