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Structure of 51549-32-7
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This purine derivative features a silylated tetrahydrofuran sugar moiety that enhances stability and solubility in organic media. The tert-butyldimethylsilyl groups protect hydroxyl functionalities, enabling straightforward incorporation into nucleoside analogs under standard conditions.
9-((2R,4S,5R)-4-((tert-Butyldimethylsilyl)oxy)-5-(((tert-butyldimethylsilyl)oxy)methyl)tetrahydrofuran-2-yl)-9H-purin-6-amine serves as a protected nucleoside building block for the synthesis of modified purine derivatives. The strategically positioned silyl ethers provide orthogonal protection, enabling selective deprotection during oligonucleotide or antiviral agent assembly. This compound exhibits excellent bench stability, facilitates efficient purification, and functions reliably in standard coupling and functionalization 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-P330-P362+P364-P405-P501
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Lot numbers can be found on the outside label of a product: