4-(3-Methyl-1H-pyrazol-1-yl)thiophene-2-boronic acid pinacol ester

95%

Reagent Code: #90390
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CAS Number 2223043-28-3

science Other reagents with same CAS 2223043-28-3

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Weight 308.20414 g/mol
Formula C₁₄H₂₁BN₂O₃S
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 synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The pyrazole moiety in the structure can contribute to the biological activity of the final products, often enhancing their efficacy in drug discovery. Additionally, it is employed in the development of materials for organic electronics, where its structural properties can influence the performance of organic semiconductors and light-emitting diodes.

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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-(3-Methyl-1H-pyrazol-1-yl)thiophene-2-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 synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The pyrazole moiety in the structure can contribute to the biological activity of the final products, often enhancing their efficacy in drug discovery. Additionally, it is employed in the deve

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 synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. The pyrazole moiety in the structure can contribute to the biological activity of the final products, often enhancing their efficacy in drug discovery. Additionally, it is employed in the development of materials for organic electronics, where its structural properties can influence the performance of organic semiconductors and light-emitting diodes.

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