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Structure of 123532-18-3
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This boronate moiety integrates a 1-methyl-1H-pyrazol-3-yl group with a phenolic hydroxyl, enabling efficient coupling in Suzuki-Miyaura reactions. The electron-rich heterocycle enhances reactivity while maintaining bench-stable handling under standard conditions.
2-(1-Methyl-1H-pyrazol-3-yl)phenol serves as a versatile building block in medicinal chemistry, enabling the construction of bioactive heterocyclic scaffolds. Its phenolic hydroxyl group facilitates direct functionalization or metal-catalyzed coupling reactions, while the 1-methylpyrazole moiety provides metabolic stability and hydrogen-bonding capability. The compound exhibits bench stability, good solubility in common organic solvents, and compatibility with standard purification methods, making it well-suited for iterative synthesis campaigns in drug discovery.
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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 : H315-H319
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Precautionary Statements : P264-P280-P302+P352-P362+P364
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Lot numbers can be found on the outside label of a product: