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Structure of 103285-22-9
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5’-O-(4,4’-Dimethoxytrityl)-2’-O-methyluridine delivers a protected nucleoside scaffold for automated oligonucleotide synthesis. The dimethoxytrityl group enables efficient 5’-end labeling and chain elongation, while the 2’-O-methyl modification enhances nuclease resistance and conformational stability in synthetic RNA analogs. This derivative supports high-fidelity incorporation under standard phosphoramidite coupling conditions.
5’-O-(4,4’-Dimethoxytrityl)-2’-O-methyluridine serves as a key building block in the synthesis of modified oligonucleotides, enabling efficient 3’→5’ phosphodiester linkage formation. The 4,4’-dimethoxytrityl group provides robust protection at the 5’-hydroxyl, facilitating controlled chain elongation and ease of purification via trityl cation monitoring. The 2’-O-methyl modification enhances nuclease resistance and improves binding affinity, making this derivative ideal for antisense and RNAi applications requiring enhanced stability and target specificity.
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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: