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Structure of 892-48-8
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5'-Chloro-5'-deoxyadenosine features a chlorine atom at the 5' position of the ribose moiety, conferring enhanced metabolic stability and resistance to enzymatic degradation. This modification enables prolonged intracellular retention and facilitates targeted incorporation into nucleic acid strands during synthetic oligonucleotide assembly. The chloro-substituted analog serves as a key building block in the development of site-specifically modified nucleoside probes for biochemical and therapeutic applications.
5'-Chloro-5'-deoxyadenosine serves as a valuable nucleoside building block for the synthesis of modified oligonucleotides and antiviral agents. Its 5'-chloro substituent enables efficient coupling in solid-phase synthesis and facilitates downstream functionalization via nucleophilic displacement. The molecule exhibits good bench stability and compatibility with standard protecting group strategies, making it a practical choice for medicinal chemistry campaigns targeting nucleoside analogs.
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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: