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Structure of 135861-56-2
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This chiral diol features a rigid, polycyclic scaffold with dual aryl substituents that confer enhanced stability and solubility in organic media. The (1R) configuration enables stereoselective transformations, while the protected hydroxyl groups facilitate controlled functionalization in synthesis. Ideal for asymmetric catalysis and complex molecule assembly.
(1R)-1-((4R,4aR,8aS)-2,6-Bis(3,4-dimethylphenyl)tetrahydro-[1,3]dioxino[5,4-d][1,3]dioxin-4-yl)ethane-1,2-diol serves as a chiral scaffold for asymmetric synthesis, leveraging its rigid, polycyclic architecture and multiple hydroxyl functionalities. The molecule exhibits bench stability and facilitates selective derivatization under standard conditions, enabling efficient construction of complex molecular frameworks. Its functional group tolerance supports downstream transformations in medicinal chemistry and catalyst design.
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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-H319
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Precautionary Statements : P264-P270-P280-P330-P501
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Lot numbers can be found on the outside label of a product: