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Structure of 1296225-26-7
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This trifluoromethyl-substituted pyrazole methanol delivers enhanced solubility and metabolic stability in synthetic intermediates. The electron-withdrawing trifluoroethyl group modulates reactivity, while the primary alcohol enables straightforward derivatization. Ideal for medicinal chemistry campaigns requiring polar, bench-stable building blocks with tailored electronic properties.
[1-(2,2,2-trifluoroethyl)-1H-pyrazol-5-yl]methanol serves as a versatile building block for medicinal chemistry and agrochemical synthesis, enabling efficient access to trifluoromethylated heterocyclic scaffolds. The aldehyde functionality facilitates reductive amination, Wittig reactions, and coupling with nucleophiles, while the pyrazole core provides metabolic stability and hydrogen-bonding capacity. Bench-stable and compatible with standard purification methods, it functions effectively in multistep syntheses requiring fluorinated aromatic motifs.
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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: