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Structure of 347194-02-9
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1-(3-(Trifluoromethoxy)phenyl)ethanol features a trifluoromethoxy-substituted phenyl ring linked to a chiral ethanol backbone, delivering enhanced lipophilicity and metabolic stability. This bench-stable scaffold integrates readily into pharmaceutical intermediates, enabling efficient access to bioactive molecules through modular derivatization pathways.
1-(3-(Trifluoromethoxy)phenyl)ethanol serves as a valuable building block in medicinal chemistry, enabling the synthesis of bioactive arylalkyl scaffolds. Its trifluoromethoxy group imparts enhanced metabolic stability and lipophilicity, while the secondary alcohol facilitates straightforward derivatization via esterification, oxidation, or protection. The compound exhibits good bench stability and is compatible with standard purification techniques, making it well-suited for iterative synthesis campaigns in API development.
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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-H335
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Precautionary Statements : P260-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: