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Structure of 859027-06-8
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This trifluoromethyl-substituted aryl alcohol features a para-nitro group that enhances electrophilicity and directs ortho-functionalization. The benzyl alcohol moiety enables direct derivatization, while the electron-deficient aromatic ring supports efficient coupling reactions under standard conditions. Ideal for constructing advanced pharmaceutical intermediates and functional materials.
(4-Nitro-2-(trifluoromethyl)phenyl)methanol serves as a versatile building block for nitroaryl-based heterocycles and pharmaceutical intermediates. Its trifluoromethyl group enhances metabolic stability and lipophilicity, while the benzylic alcohol enables straightforward derivatization via oxidation, protection, or coupling reactions. The molecule exhibits good bench stability and facilitates efficient purification, making it well-suited for scalable synthesis in medicinal chemistry campaigns.
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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: