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Structure of 882-59-7
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2,2-Diphenyloxirane features a strained epoxide ring flanked by two aryl groups, conferring high reactivity toward nucleophiles. This bench-stable compound integrates readily into asymmetric synthesis and serves as a chiral building block in catalytic transformations.
2,2-Diphenyloxirane serves as a stable, bench-ready epoxide building block for stereoselective transformations. Its electron-rich aromatic substituents enhance regioselective ring-opening reactions with nucleophiles, enabling efficient access to functionalized 1,2-diols and β-hydroxy carbonyl derivatives. The compound exhibits excellent functional group tolerance and facilitates downstream derivatization in complex molecule synthesis, making it a practical choice for medicinal chemistry and process development 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-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: