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Structure of 28708-32-9
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This triacetate derivative of tetrahydrofuran triol serves as a key protecting group strategy in carbohydrate synthesis, offering enhanced stability and controlled deprotection under mild conditions. The (3R,4R,5R) stereochemistry ensures predictable stereoselective transformations, while the acetoxymethyl side chain enables selective functionalization.
(3R,4R,5R)-5-(Acetoxymethyl)tetrahydrofuran-2,3,4-triyl triacetate serves as a key chiral building block in the synthesis of complex carbohydrate derivatives and nucleoside analogs. Its triacetate functionality provides enhanced stability and facilitates selective deprotection sequences, enabling controlled access to diol intermediates. The molecule exhibits excellent bench stability and functional group tolerance, allowing straightforward integration into multi-step syntheses involving glycosylation, coupling, or cyclization reactions.
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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: