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(E)-but-2-enoic acid [(2R,3S,5R)-5-(2,4-diketo-5-methyl-pyrimidin-1-yl)-3-hydroxy-tetrahydrofuran-2-yl]methyl ester

Compound with spectra: 1 NMR, and 1 MS (GC)

(E)-but-2-enoic acid [(2R,3S,5R)-5-(2,4-diketo-5-methyl-pyrimidin-1-yl)-3-hydroxy-tetrahydrofuran-2-yl]methyl ester
SpectraBase Compound ID 9ricEegveOm
InChI InChI=1S/C14H18N2O6/c1-3-4-12(18)21-7-10-9(17)5-11(22-10)16-6-8(2)13(19)15-14(16)20/h3-4,6,9-11,17H,5,7H2,1-2H3,(H,15,19,20)/b4-3+/t9-,10+,11+/m0/s1
InChIKey VENSHNMUBBRHOX-BJPDOBEOSA-N
Mol Weight 310.31 g/mol
Molecular Formula C14H18N2O6
Exact Mass 310.116486 g/mol
Enantiomer InChIKey VENSHNMUBBRHOX-QDVNPKLESA-N

View Spectrum of (E)-but-2-enoic acid [(2R,3S,5R)-5-(2,4-diketo-5-methyl-pyrimidin-1-yl)-3-hydroxy-tetrahydrofuran-2-yl]methyl ester

MS (GC) Spectrum
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Source of Spectrum J-58-659-3

View Spectrum of (E)-but-2-enoic acid [(2R,3S,5R)-5-(2,4-diketo-5-methyl-pyrimidin-1-yl)-3-hydroxy-tetrahydrofuran-2-yl]methyl ester

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
  • [(2R,3S,5R)-3-hydroxy-5-(5-methyl-2,4-dioxo-pyrimidin-1-yl)tetrahydrofuran-2-yl]methyl (E)-but-2-enoate
acrylic acid [(2R,3S,5R)-5-(2,4-diketo-5-methyl-pyrimidin-1-yl)-3-hydroxy-tetrahydrofuran-2-yl]methyl ester
1-Thymine-2-deoxy-.beta.-D-ribofuranos-5-yl 2-Propenoate
2-chloroacetic acid [(2R,3S,5R)-5-(2,4-diketo-5-methyl-pyrimidin-1-yl)-3-hydroxy-tetrahydrofuran-2-yl]methyl ester
butyric acid [(2R,3S,5R)-5-(2,4-diketo-5-methyl-pyrimidin-1-yl)-3-hydroxy-tetrahydrofuran-2-yl]methyl ester
1-Thymine-2-deoxy-.beta.-D-ribofuranos-5-yl Butanoate
5'-O-PIVALOYL-THYMIDINE
caprylic acid [(2R,3S,5R)-5-(2,4-diketo-5-methyl-pyrimidin-1-yl)-3-hydroxy-tetrahydrofuran-2-yl]methyl ester
1-Thymine-2-deoxy-.beta.-D-ribofuranos-5-yl Decanoate
5'-O-CARBAZOYLTHIMIDINE
[(2R,3S,5R)-3-hydroxy-5-(5-methyl-2,4-dioxo-pyrimidin-1-yl)tetrahydrofuran-2-yl]methyl vinyl carbonate
Title Journal or Book Year
A useful and versatile procedure for the acylation of nucleosides through an enzymic reaction The Journal of Organic Chemistry 1993
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