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Structure of 32345-59-8
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(R)-Methyl 2-(2-chlorophenyl)-2-hydroxyacetate is a chiral building block featuring a stereodefined hydroxyl group adjacent to a carbonyl, enabling precise functionalization in asymmetric synthesis. The ortho-chlorophenyl moiety imparts enhanced reactivity and stability under standard bench conditions. This compound integrates readily into pharmaceutical intermediates and complex molecular architectures requiring controlled stereochemistry.
(R)-Methyl 2-(2-chlorophenyl)-2-hydroxyacetate serves as a chiral building block for the synthesis of biologically relevant heterocycles and pharmaceutical intermediates. Its well-defined stereochemistry enables stereoselective transformations, while the α-hydroxy ester functionality supports facile derivatization via oxidation, reduction, or coupling reactions. Bench-stable and readily purified by chromatography, it functions effectively in multi-step syntheses requiring high enantiomeric purity and functional group compatibility.
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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
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Precautionary Statements : P264-P270-P330
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Lot numbers can be found on the outside label of a product: