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

97%

Reagent Code: #242724
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CAS Number 1093307-35-7

science Other reagents with same CAS 1093307-35-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 233.07 g/mol
Formula C₁₁H₁₆BN₃O₂
badge Registry Numbers
MDL Number MFCD18383259
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used primarily in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions. Its pyrazole and nitrile functionalities make it valuable for constructing biologically active molecules, particularly in pharmaceutical and agrochemical research. The compound enables efficient formation of carbon-carbon bonds, facilitating the development of complex heterocyclic systems. It is also employed in the synthesis of functional materials and ligands for catalysis due to its stable boronate group and reactive nitrile moiety.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,820.00
inventory 250mg
10-20 days ฿4,290.00
inventory 1g
10-20 days ฿10,890.00
inventory 5g
10-20 days ฿41,520.00

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2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)acetonitrile
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Used primarily in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions. Its pyrazole and nitrile functionalities make it valuable for constructing biologically active molecules, particularly in pharmaceutical and agrochemical research. The compound enables efficient formation of carbon-carbon bonds, facilitating the development of complex heterocyclic systems. It is also employed in the synthesis of functional materials and ligands for catalysis due to its stab

Used primarily in organic synthesis as a boronic ester coupling partner in Suzuki-Miyaura cross-coupling reactions. Its pyrazole and nitrile functionalities make it valuable for constructing biologically active molecules, particularly in pharmaceutical and agrochemical research. The compound enables efficient formation of carbon-carbon bonds, facilitating the development of complex heterocyclic systems. It is also employed in the synthesis of functional materials and ligands for catalysis due to its stable boronate group and reactive nitrile moiety.

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