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Structure of 61008-98-8
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(R)-2-(3-Chlorophenyl)-2-hydroxyacetic acid features a chiral center flanked by a hydroxyl group and a 3-chlorophenyl moiety, delivering enhanced stereochemical control in asymmetric synthesis. The electron-withdrawing chlorine substituent stabilizes adjacent carbanions, enabling efficient functionalization under mild conditions. This bench-stable, moisture-tolerant reagent integrates seamlessly into pharmaceutical intermediates and chiral building block workflows.
(R)-2-(3-Chlorophenyl)-2-hydroxyacetic acid serves as a valuable chiral building block for synthesizing pharmaceutical intermediates and bioactive heterocycles. Its well-defined stereochemistry and carboxylic acid functionality enable straightforward derivatization, including esterification and amide coupling, while the ortho-chlorophenyl group provides a handle for further functionalization via cross-coupling reactions. The compound exhibits good bench stability and is readily purified by recrystallization, making it suitable for scalable synthesis 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-P280-P302+P352
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Lot numbers can be found on the outside label of a product: