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Structure of 3416-05-5
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3′-Deoxythymidine is a nucleoside analog featuring a modified sugar moiety that lacks the 3′-hydroxyl group, rendering it incapable of forming phosphodiester bonds in DNA chains. This structural feature enables its use as a chain terminator in nucleic acid synthesis studies and antiviral research, particularly in investigating reverse transcriptase activity. The compound exhibits stability under standard laboratory conditions and integrates readily into oligonucleotide sequences for mechanistic probing.
3′-Deoxythymidine serves as a valuable nucleoside building block in the synthesis of antiviral agents and oligonucleotide analogs. Its modified sugar moiety enhances metabolic stability while retaining compatibility with standard phosphoramidite coupling protocols. The 3′-deoxy configuration prevents chain elongation, making it useful for controlled oligonucleotide synthesis and mechanistic studies of polymerase 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: