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Structure of 137536-94-8
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This chiral dioxolane diol features two naphthalen-1-ylmethyl groups positioned at the 4,5-aryl sites, delivering enhanced rigidity and steric shielding. The (4R,5R) stereochemistry ensures predictable conformational behavior in asymmetric synthesis. Designed for stability under standard conditions, it integrates seamlessly into complex molecular architectures requiring defined spatial orientation and resistance to racemization.
((4R,5R)-2,2-Dimethyl-1,3-dioxolane-4,5-diyl)bis(di(naphthalen-1-yl)methanol) serves as a stereochemically defined chiral synthon for the construction of complex polyfunctionalized heterocycles. Its rigid dioxolane framework provides excellent bench stability and facilitates orthogonal functional group manipulation. The di(naphthalen-1-yl)methanol moieties enable efficient coupling reactions and offer enhanced solubility in organic media, supporting scalable transformations in medicinal chemistry and natural product synthesis.
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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: