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acetic acid [(2R,3R,4S,5R)-5-(4-acetamido-2-keto-pyrimidin-1-yl)-4-acetoxy-2-(acetoxymethyl)tetrahydrofuran-3-yl] ester

Compound with spectra: 1 NMR

acetic acid [(2R,3R,4S,5R)-5-(4-acetamido-2-keto-pyrimidin-1-yl)-4-acetoxy-2-(acetoxymethyl)tetrahydrofuran-3-yl] ester
SpectraBase Compound ID 3auy6Dml3Ji
InChI InChI=1S/C17H21N3O9/c1-8(21)18-13-5-6-20(17(25)19-13)16-15(28-11(4)24)14(27-10(3)23)12(29-16)7-26-9(2)22/h5-6,12,14-16H,7H2,1-4H3,(H,18,19,21,25)/t12-,14-,15+,16-/m1/s1
InChIKey SABGQSSAGOWXJK-DMRZNYOFSA-N
Mol Weight 411.37 g/mol
Molecular Formula C17H21N3O9
Exact Mass 411.127779 g/mol
Enantiomer InChIKey SABGQSSAGOWXJK-HNKHHVNMSA-N

View Spectrum of acetic acid [(2R,3R,4S,5R)-5-(4-acetamido-2-keto-pyrimidin-1-yl)-4-acetoxy-2-(acetoxymethyl)tetrahydrofuran-3-yl] ester

13C NMR Spectrum
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Solvent CDCl3
N(6)-Acetyl-2',3',5'-tri-0-acetylcytidine
Cytidine, N-acetyl-, 2',3',5'-triacetate
BWPKOVBKNIGFLC-WNHJNPCNSA-N
Benzamide, N-[1-(2,3-di-O-acetyl-.beta.-D-arabinofuranosyl)-1,2-dihydro-2-oxo-4-pyrimidinyl]-4-methoxy-
QVPKKJQERLOSQJ-LEAZDLGRSA-N
OKWFGDIDUPKZFV-UKMLZYKCSA-N
FLUOROURIDINE-TRIACETATE
2',3'-O-ISOPROPYLIDENE-4-N-ACETYL-CYTIDINE
2',3'-DI-O-ACETYLURIDINE-5'-O-ACETYLPHOSPHATE
2',5'-DI-O-ACETYLURIDINE, 3'-PHOSPHATE
Title Journal or Book Year
Differential reactivity of carbohydrate hydroxyls in glycosylations. II. The likely role of intramolecular hydrogen bonding on glycosylation reactions. Galactosylation of nucleoside 5′-hydroxyls for the syntheses of novel potential anticancer agents Canadian Journal of Chemistry 1994
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