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Structure of 1206550-93-7
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Ethyl 2-(4-(trifluoromethoxy)phenyl)acetate features a trifluoromethoxy-substituted phenyl ring conjugated to an acetic acid ester, delivering enhanced electron-withdrawing character and improved metabolic stability. This moiety integrates readily into pharmaceutical intermediates requiring lipophilic, fluorinated aromatic components. The ethyl ester group enables straightforward functionalization under standard conditions.
Ethyl 2-(4-(trifluoromethoxy)phenyl)acetate serves as a versatile building block for pharmaceutical and agrochemical synthesis, enabling efficient access to biologically relevant arylacetic acid derivatives. The trifluoromethoxy group enhances metabolic stability and modulates lipophilicity, while the ester functionality allows for straightforward hydrolysis or further functionalization. This compound exhibits excellent bench stability, tolerates a range of reaction conditions, and facilitates coupling reactions in standard synthetic 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: