2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)acetamide

95%

Reagent Code: #240858
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CAS Number 1083326-46-8

science Other reagents with same CAS 1083326-46-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 251.09 g/mol
Formula C₁₁H₁₈BN₃O₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used primarily in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions. Its pyrazole core with an acetamide side chain makes it valuable for constructing biologically active molecules, particularly in pharmaceutical and agrochemical research. The compound enables the formation of carbon-carbon bonds under mild conditions, facilitating the development of complex heterocyclic systems. It is especially useful in the synthesis of kinase inhibitors and other drug-like molecules where the pyrazole moiety is a key pharmacophore. The presence of the amide group allows for further functionalization or hydrogen bonding interactions in target compounds.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿420.00
inventory 100mg
10-20 days ฿1,000.00
2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)acetamide
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Used primarily in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions. Its pyrazole core with an acetamide side chain makes it valuable for constructing biologically active molecules, particularly in pharmaceutical and agrochemical research. The compound enables the formation of carbon-carbon bonds under mild conditions, facilitating the development of complex heterocyclic systems. It is especially useful in the synthesis of kinase inhibitors and other drug-li

Used primarily in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions. Its pyrazole core with an acetamide side chain makes it valuable for constructing biologically active molecules, particularly in pharmaceutical and agrochemical research. The compound enables the formation of carbon-carbon bonds under mild conditions, facilitating the development of complex heterocyclic systems. It is especially useful in the synthesis of kinase inhibitors and other drug-like molecules where the pyrazole moiety is a key pharmacophore. The presence of the amide group allows for further functionalization or hydrogen bonding interactions in target compounds.

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