1-Ethyl-3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole

95%

Reagent Code: #185181
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CAS Number 1876473-39-0

science Other reagents with same CAS 1876473-39-0

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Storage -20°C, Inert Gas

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Used primarily in cross-coupling reactions, this compound serves as a key boronic ester reagent in Suzuki-Miyaura coupling, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its pyrazole core is valuable for constructing nitrogen-containing heterocycles, commonly found in bioactive molecules. The presence of the dioxaborolane group ensures good stability and reactivity under palladium catalysis, making it suitable for late-stage functionalization in drug discovery. It is also employed in materials science for building conjugated systems in organic electronics due to its reliable coupling efficiency and structural versatility.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,020.00
inventory 250mg
10-20 days ฿6,930.00
inventory 1g
10-20 days ฿19,200.00

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1-Ethyl-3-methyl-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
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Used primarily in cross-coupling reactions, this compound serves as a key boronic ester reagent in Suzuki-Miyaura coupling, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its pyrazole core is valuable for constructing nitrogen-containing heterocycles, commonly found in bioactive molecules. The presence of the dioxaborolane group ensures good stability and reactivity under palladium catalysis, making it suitable for late-stage functionalization in drug discover

Used primarily in cross-coupling reactions, this compound serves as a key boronic ester reagent in Suzuki-Miyaura coupling, enabling the formation of carbon-carbon bonds in pharmaceutical and agrochemical synthesis. Its pyrazole core is valuable for constructing nitrogen-containing heterocycles, commonly found in bioactive molecules. The presence of the dioxaborolane group ensures good stability and reactivity under palladium catalysis, making it suitable for late-stage functionalization in drug discovery. It is also employed in materials science for building conjugated systems in organic electronics due to its reliable coupling efficiency and structural versatility.

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