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Structure of 1093307-35-7
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This boronate-functionalized pyrazole derivative integrates seamlessly into cross-coupling reactions, delivering efficient access to complex heteroaryl nitriles. The tetramethylboronate moiety enables stable, room-temperature handling and high reactivity under palladium catalysis, while the acetonitrile group provides a polar anchor for downstream derivatization and enhanced solubility in common organic solvents.
2-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl)acetonitrile serves as a versatile boronate building block for Suzuki-Miyaura cross-coupling reactions. The pyrazole moiety provides a stable heterocyclic scaffold with defined regiochemistry, while the nitrile group offers orthogonal reactivity for downstream functionalization. Bench-stable and compatible with standard coupling conditions, it enables efficient construction of biologically relevant pyrazole-containing architectures in medicinal chemistry and materials science applications.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: