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Structure of 4254-15-3
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(S)-(+)-1,2-Propanediol can be used as a reactant to synthesize:Optically active chiral (S)-1, 2-propanediol derivatives using mesogenic carboxylic acids via esterification in the presence of dimethylaminopyridine (DMAP) as a catalyst.3,4-Ethylenedioxythiophenes via Mitsunobu reaction.Vicinal diol cyclic sulfates in the presence of sodium periodate and ruthenium chloride as catalysts.
(S)-(+)-1,2-Propanediol serves as a chiral synthon in asymmetric synthesis, offering reliable stereocontrol in nucleophilic additions and epoxide formations. Its bench-stable, low-moisture-sensitive nature facilitates straightforward handling and purification. Widely employed in the construction of heterocyclic scaffolds and bioactive intermediates, it functions effectively in esterification, etherification, and metal-catalyzed coupling reactions with high functional group tolerance.
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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: