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Structure of 23585-51-5
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This bench-stable pyrazole derivative features a tertiary alcohol group flanked by a pyrazolyl ring, enabling straightforward functionalization in synthetic routes. The electron-rich heterocycle enhances reactivity in transition metal-catalyzed couplings and provides a rigid scaffold for molecular diversity in medicinal chemistry applications.
2-(1H-Pyrazol-3-yl)propan-2-ol serves as a stable, bench-ready building block for the synthesis of bioactive heterocycles. Its tertiary alcohol functionality enables straightforward derivatization, while the pyrazole ring provides orthogonal reactivity and enhanced solubility. The molecule functions effectively in coupling reactions and serves as a versatile scaffold in medicinal chemistry campaigns targeting kinase inhibitors and CNS modulators.
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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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: