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Structure of 1082503-77-2
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This boronate-functionalized pyrazole integrates readily into Suzuki-Miyaura coupling reactions under standard conditions, offering high stability and compatibility with diverse reaction environments. The tetramethyl-1,3,2-dioxaborolane moiety enables efficient cross-coupling, while the tertiary alcohol scaffold provides steric protection and enhanced solubility in polar aprotic solvents.
2-Methyl-1-[4-(tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazol-1-yl]propan-2-ol serves as a stable, bench-ready boronate building block for Suzuki-Miyaura cross-coupling reactions. The tetramethylboronate moiety enables efficient coupling with aryl and heteroaryl halides under mild conditions, while the pyrazole core provides a versatile scaffold for medicinal chemistry applications. Its tertiary alcohol functionality enhances solubility and facilitates purification, making it well-suited for iterative synthesis of complex molecular architectures.
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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: