This compound is a protected nucleoside intermediate used in the synthesis of oligonucleotides. Its structure features a bicyclic sugar moiety and a benzamide-protected pyrimidine base, making it suitable for solid-phase or solution-phase oligonucleotide assembly.
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N6-BENZOYL-2'-O-METHYL-ADENOSINE
nucleoside intermediate for oligonucleotide synthesis
N-(9-((2R,3R,4R,5R)-5-((Bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-hydroxy-3-methoxytetrahydrofuran-2-yl)-9H-purin-6-yl)benzamide
nucleoside intermediate for oligonucleotide synthesis
N-(1-((2R,3R,4R,5R)-5-((Bis(4-methoxyphenyl)(phenyl)methoxy)methyl)-4-hydroxy-3-methoxytetrahydrofuran-2-yl)-2-oxo-1,2-dihydropyrimidin-4-yl)acetamide
nucleoside intermediate for oligonucleotide synthesis
2-Methoxy-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)pyridine
Pharmaceutical intermediate for boron-containing compounds
3,4-Dihydro-2-methoxy-2H-pyran
Chemical intermediate for synthesis
Ethyl (methylthio)acetate
Pharmaceutical intermediate
4-Nitrobenzyl chloroformate
protecting group reagent
(1R,3R,4R,7S)-3-(4-N-Benzoyl-5-methylcytosin-1-yl)-7-(2-cyanoethoxy(diisopropylamino)phosphinoxy)-1-(4,4'-dimethoxytrityloxymethyl)-2,5-dioxabicyclo(2.2.1)heptane
oligonucleotide synthesis building block
N-[1-[(1R,3R,4R,7S)-1-[[bis(4-methoxyphenyl)-phenylmethoxy]methyl]-7-hydroxy-2,5-dioxabicyclo[2.2.1]heptan-3-yl]-5-methyl-2-oxopyrimidin-4-yl]benzamide
CTGWFRQUULNNIN-OSZGUBSQSA-N
CC1=CN(C(=O)N=C1NC(=O)C2=CC=CC=C2)[C@H]3[C@H]4[C@@H]([C@@](O3)(CO4)COC(C5=CC=CC=C5)(C6=CC=C(C=C6)OC)C7=CC=C(C=C7)OC)O
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