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

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Reagent Code: #197197
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CAS Number 1619991-78-4

science Other reagents with same CAS 1619991-78-4

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Used as a key intermediate in cross-coupling reactions, particularly in Suzuki-Miyaura coupling, to construct complex pyrazole-based structures. Its boron-containing group enables efficient carbon-carbon bond formation, making it valuable in pharmaceutical and agrochemical synthesis where pyrazole motifs are common. The compound supports the development of active ingredients in crop protection agents and medicinal candidates due to its stability and reactivity under mild conditions. It is especially useful in late-stage functionalization, allowing chemists to introduce diverse substituents into heterocyclic systems.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿12,700.00
inventory 250mg
10-20 days ฿25,380.00
inventory 1g
10-20 days ฿43,240.00

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3-ethyl-1-methyl-4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole
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Used as a key intermediate in cross-coupling reactions, particularly in Suzuki-Miyaura coupling, to construct complex pyrazole-based structures. Its boron-containing group enables efficient carbon-carbon bond formation, making it valuable in pharmaceutical and agrochemical synthesis where pyrazole motifs are common. The compound supports the development of active ingredients in crop protection agents and medicinal candidates due to its stability and reactivity under mild conditions. It is especially usef

Used as a key intermediate in cross-coupling reactions, particularly in Suzuki-Miyaura coupling, to construct complex pyrazole-based structures. Its boron-containing group enables efficient carbon-carbon bond formation, making it valuable in pharmaceutical and agrochemical synthesis where pyrazole motifs are common. The compound supports the development of active ingredients in crop protection agents and medicinal candidates due to its stability and reactivity under mild conditions. It is especially useful in late-stage functionalization, allowing chemists to introduce diverse substituents into heterocyclic systems.

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