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Structure of 39824-26-5
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6-Chloro-9-[2,3-O-(1-methylethylidene)-beta-D-ribofuranosyl]-9H-Purine features a protected ribose moiety that enhances stability and facilitates controlled incorporation into nucleic acid analogs. The chlorinated purine base supports efficient coupling in oligonucleotide synthesis workflows, offering improved resistance to hydrolysis under standard conditions.
6-Chloro-9-[2,3-O-(1-methylethylidene)-β-D-ribofuranosyl]-9H-purine serves as a key nucleoside building block for the synthesis of antiviral agents and purine-based pharmaceutical intermediates. The protected ribose moiety enhances stability and facilitates selective functionalization at the C-6 position. Its well-documented reactivity enables reliable glycosylation and coupling protocols in medicinal chemistry workflows, supporting scalable synthesis of nucleoside analogs with proven biological activity.
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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: