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Structure of 126534-42-7
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(S)-1-Chloro-2-hydroxy-2-(p-fluorophenyl)ethane features a chiral center with defined stereochemistry, enabling precise asymmetric synthesis. The para-fluorophenyl group imparts enhanced electron-withdrawing character, while the hydroxyl moiety offers a reactive handle for derivatization. This bench-stable compound serves as a key intermediate in pharmaceutical and agrochemical route development.
(S)-1-Chloro-2-hydroxy-2-(p-fluorophenyl)ethane serves as a versatile chiral building block in synthetic organic chemistry, enabling stereoselective transformations through its adjacent chloro and hydroxyl functionalities. The molecule exhibits bench stability and facilitates efficient functional group interconversions, including nucleophilic substitution and oxidation reactions. Its ortho-substituted aryl moiety enhances structural rigidity and provides a handle for further derivatization in the synthesis of bioactive compounds and pharmaceutical intermediates.
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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: