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Structure of 1294481-82-5
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This nucleoside analog features a fluorinated oxolane ring bearing a chlorobenzoyloxy methyl group and a 2-amino-6-chloro-9H-purin-9-yl moiety, delivering enhanced stability and targeted bioavailability. The 4-chlorobenzoate ester facilitates controlled release in biological systems.
This compound serves as a key nucleoside analog intermediate, enabling efficient synthesis of purine-based building blocks. The protected hydroxyl groups and orthogonal functionalization support reliable glycosylation and derivatization workflows. Bench-stable and amenable to standard purification methods, it facilitates scalable access to antiviral and anticancer scaffolds through established coupling and deprotection protocols.
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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: