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Structure of 108998-83-0
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This chiral diol features a rigid, sterically congested triphenylmethyl backbone that stabilizes adjacent hydroxyl groups. The (2S) configuration imparts distinct stereochemical control in asymmetric synthesis, enabling selective functionalization without racemization. Ideal for building complex architectures in medicinal chemistry and catalytic design.
(2S)-1,1,2-Triphenylethane-1,1,2-triol serves as a chiral synthon in asymmetric synthesis, enabling stereoselective transformations via its rigid, enantiomerically pure scaffold. The adjacent hydroxyl groups facilitate selective derivatization and oxidation reactions, while the triphenyl substitution enhances bench stability and simplifies purification. Functions effectively in catalytic asymmetric processes and as a building block for complex heterocyclic systems.
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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: