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Structure of 99226-02-5
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trans-2-(2-Methoxyphenyl)-5-oxotetrahydrofuran-3-carboxylic acid features a rigid, electron-deficient tetrahydrofuran core fused to an aromatic methoxyphenyl group. This configuration enhances metabolic stability and facilitates selective conjugation in synthetic intermediates. The carboxylic acid moiety enables direct coupling without additional activation, streamlining access to bioactive scaffolds under standard conditions.
trans-2-(2-Methoxyphenyl)-5-oxotetrahydrofuran-3-carboxylic acid serves as a versatile chiral building block in synthetic organic chemistry, enabling access to substituted tetrahydrofuran scaffolds via standard functional group interconversions. Its bench-stable nature and defined stereochemistry facilitate reliable use in multistep synthesis, particularly for constructing bioactive heterocycles and medicinal chemistry 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: