CCOP(=O)(OCC)C([C@@H]1O[C@@H]([C@@H](O[Si](C)(C)C(C)(C)C)[C@H]1O[Si](C)(C)C(C)(C)C)N1C=CC(=O)NC1=O)N(C)O

InChIKey=GVMMZICIWHTCDA-QAROPEJJSA-N

C26H52N3O9PSi2

637.858

Organic compounds

Nucleosides, nucleotides, and analogues

5'-deoxyribonucleosides

Not available

Not available

5'-deoxyribonucleosides

Glycosylamines Pyrimidones Dialkyl alkylphosphonates Phosphonic acid esters Hydropyrimidines Vinylogous amides Trialkylheterosilanes Oxolanes Heteroaromatic compounds Ureas Silyl ethers Lactams Oxacyclic compounds Azacyclic compounds Organic metalloid salts N-organohydroxylamines Hydrocarbon derivatives Organic oxides Organophosphorus compounds

Aromatic heteromonocyclic compounds

5'-deoxyribonucleoside - Glycosyl compound - N-glycosyl compound - Dialkyl alkylphosphonate - Pyrimidone - Phosphonic acid diester - Hydropyrimidine - Phosphonic acid ester - Pyrimidine - Trialkylheterosilane - Organophosphonic acid derivative - Oxolane - Heteroaromatic compound - Vinylogous amide - Lactam - Urea - Silyl ether - N-organohydroxylamine - Azacycle - Oxacycle - Organoheterosilane - Organic metalloid salt - Organoheterocyclic compound - Organosilicon compound - Organic nitrogen compound - Hydrocarbon derivative - Organophosphorus compound - Organooxygen compound - Organonitrogen compound - Organic oxide - Organic metalloid moeity - Organic oxygen compound - Aromatic heteromonocyclic compound

This compound belongs to the class of organic compounds known as 5'-deoxyribonucleosides. These are nucleosides in which the oxygen atom at the 5'position of the ribose moiety has been replaced by another atom. The nucleobases here are limited to purine, pyrimidine, and pyridine derivatives.

Not available