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Structure of 136834-21-4
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DMT-2'-F-Bz-dA is a protected nucleoside building block featuring a 2'-fluorinated sugar and a benzoyl group at the 5'-position, enabling efficient incorporation into oligonucleotide synthesis. The dimethoxytrityl (DMT) group at the 5'-end facilitates purification and monitoring during solid-phase assembly. This derivative combines enhanced nuclease resistance with improved hybridization affinity, making it ideal for antisense and siRNA applications.
DMT-2'-F-Bz-dA serves as a key building block for the synthesis of modified oligonucleotides, enabling site-specific incorporation of 2'-fluoro and benzoyl-protected deoxyadenosine residues. The DMT group provides orthogonal protection for the 5'-OH, facilitating efficient solid-phase synthesis, while the 2'-F substituent enhances nuclease resistance and duplex stability. The benzoyl group offers reliable protection during coupling steps, with straightforward removal under mild basic conditions. This derivative is particularly valuable in the construction of antisense oligonucleotides and nucleic acid therapeutics requiring enhanced metabolic stability and binding affinity.
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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: