Lot numbers can be found on the outside label of a product:
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Structure of 827-99-6
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3-(Trifluoromethoxy)phenol features a trifluoromethoxy group attached to the meta position of a phenolic ring, delivering enhanced electron-withdrawing character and improved metabolic stability. This combination imparts strong solubility in organic solvents and resistance to oxidation under standard handling conditions. The compound serves as a key building block in the synthesis of pharmaceutical intermediates, agrochemicals, and functional materials requiring fluorinated aromatic motifs.
3-(Trifluoromethoxy)phenol serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient access to bioactive heterocycles through standard electrophilic substitution and coupling reactions. Its trifluoromethoxy group imparts enhanced metabolic stability and lipophilicity, while the phenolic functionality offers direct handle for derivatization via etherification, esterification, or metal-catalyzed cross-coupling. The compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for scalable synthesis and high-throughput screening workflows.
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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: