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(1R,7S)-4-(PROP-2'-ENYLOXY)-3,5,8-TRIOXA-4,LAMBDA[5]-PHOSPHABICYCLO-[5.3.0]-DECAN-4,9-DIONE;SECOND-CONFORMERE

Compound with spectra: 2 NMR

(1R,7S)-4-(PROP-2'-ENYLOXY)-3,5,8-TRIOXA-4,LAMBDA[5]-PHOSPHABICYCLO-[5.3.0]-DECAN-4,9-DIONE;SECOND-CONFORMERE
SpectraBase Compound ID Dx2f0G7XHm
InChI InChI=1S/C9H13O6P/c1-2-3-12-16(11)13-5-7-4-9(10)15-8(7)6-14-16/h2,7-8H,1,3-6H2/t7-,8-,16?/m0/s1
InChIKey WCQYMEYOBLFDPH-UBJYMUIPSA-N
Mol Weight 248.17 g/mol
Molecular Formula C9H13O6P
Exact Mass 248.044975 g/mol
Enantiomer InChIKey WCQYMEYOBLFDPH-RACNGCFMSA-N

View Spectrum of (1R,7S)-4-(PROP-2'-ENYLOXY)-3,5,8-TRIOXA-4,LAMBDA[5]-PHOSPHABICYCLO-[5.3.0]-DECAN-4,9-DIONE;SECOND-CONFORMERE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of (1R,7S)-4-(PROP-2'-ENYLOXY)-3,5,8-TRIOXA-4,LAMBDA[5]-PHOSPHABICYCLO-[5.3.0]-DECAN-4,9-DIONE;SECOND-CONFORMERE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (1R,7S)-4-(PROP-2'-ENYLOXY)-3,5,8-TRIOXY-4,LAMBDA[5]-PHOSPHABICYCLO-[5.3.0]-DECAN-4,9-DIONE;FIRST-CONFORMERE
1,2-DISTEAROYL-3-RAC-GLYCEROPHOSPHORYL-2'-BENZYLOXYHOMOCHOLINE
(2R,3S)-PHOSPHORIC-ACID-DIBENZYLESTER-2,3-BIS-(BENZYLOXY)-4-OXOBUTYLESTER
Phosphoric acid (2R,3S,5R)-5-bromomethyl-2-methyl-tetrahydro-furan-3-yl ester diphenyl ester
2-(DIPHENYLMETHYLSILYL)-ETHYL-BIS-(2,3-O-ISOPROPYLIDENE-SN-GLYCERO-1-)-PHOSPHATE
.ALPHA.-D-FRUCTOFURANOSE, 6-(DIHYDROGEN PHOSPHATE)
(PENTAETHYLENEGLYCO)-PHOSPHO-1-MYO-INOSITOL
ALPHA/BETA-D-XYLOFURANOSIDE-2,5-DIPHOSPHATE-BIS-SODIUM-SALT
2-DEOXY-2-FLUORO-D-GLUCOSE-6-PHOSPHATE-POTASSIUM-SALT
SN-GLYCERO-3-PHOSPHO-(1'-MYO-INOSITOL)
2-AMINO-2-DEOXY-D-GLUCOSE, 6-(DIHYDROGEN PHOSPHATE), BARIUM SALT, DIHYDRATE
Title Journal or Book Year
The synthesis of novel 3′,5′-homocyclic nucleotides as potential anti-HIV agents Journal of the Chemical Society, Perkin Transactions 1 1999
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