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Structure of 243977-23-3
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This trifluoromethylthio-substituted acetic acid derivative features a robust aryl-thio linkage that enhances metabolic stability and lipophilicity. The para-positioned trifluoromethylthio group imparts strong electron-withdrawing character, enabling precise tuning of reactivity in synthetic transformations. Designed for medicinal chemistry applications, this compound integrates seamlessly into bioactive scaffolds requiring enhanced membrane permeability and resistance to oxidative degradation.
2-(4-((Trifluoromethyl)thio)phenyl)acetic acid serves as a versatile building block in medicinal chemistry, enabling the synthesis of bioactive molecules through standard functional group transformations. Its trifluoromethylthio moiety imparts enhanced metabolic stability and lipophilicity, while the carboxylic acid functionality facilitates direct coupling or derivatization. The compound exhibits good bench stability and is compatible with common reaction conditions, supporting efficient access to heterocyclic scaffolds and API intermediates.
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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: