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Structure of 7403-25-0
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This nucleoside analog features a tetrahydrofuran sugar moiety with stereochemistry at the 2S,3S,5R positions, enabling precise incorporation into oligonucleotide synthesis. The pendant amino group and purine base facilitate hydrogen bonding in duplex structures, while the primary alcohol supports efficient derivatization. Bench-stable under standard conditions, it serves as a key building block for modified DNA/RNA constructs.
((2S,3S,5R)-3-Amino-5-(6-amino-9H-purin-9-yl)tetrahydrofuran-2-yl)methanol serves as a key nucleoside scaffold building block, enabling efficient synthesis of purine-based analogs. Its tetrahydrofuran core provides stereochemical control and enhanced stability, while the amino and hydroxymethyl functionalities offer versatile handles for phosphorylation, glycosylation, and coupling reactions. The molecule exhibits robust bench stability and facilitates straightforward purification, making it well-suited for iterative medicinal chemistry campaigns targeting antiviral and anticancer agents.
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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
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Precautionary Statements : P264-P270-P330-P501
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Lot numbers can be found on the outside label of a product: