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VBHLKZHSCMQLTI-UHFFFAOYSA-N
SpectraBase Compound ID 3g7ZORI4b9A
InChI InChI=1S/C12H15N5O5/c1-7(18)14-12-15-10-9(11(20)16-12)13-5-17(10)6-21-3-4-22-8(2)19/h5H,3-4,6H2,1-2H3,(H2,14,15,16,18,20)
InChIKey VBHLKZHSCMQLTI-UHFFFAOYSA-N
Mol Weight 309.28 g/mol
Molecular Formula C12H15N5O5
Exact Mass 309.107319 g/mol
Copyright Copyright © 2016-2024 Chemical Block, Russia, Leninsky Prospect 47 - Database Compilation Copyright © 2016-2021 John Wiley & Sons, Inc. All Rights Reserved.
Solvent DMSO-d6
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent Unknown
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
  • N2-ACETYL-9-(2-ACETOXYETHOXYMETHYL)-GUANINE
  • 9-[(2-ACETOXYETHOXY)-METHYL]-N(2)-ACETYLGUANINE
  • acetamide, N-[9-[[2-(acetyloxy)ethoxy]methyl]-6,9-dihydro-6-oxo-1H-purin-2-yl]-
Title Journal or Book Year
NMR spectral data for acyclovir prodrugs Magnetic Resonance in Chemistry 1999
A Simple Solution to the Age Old Problem of Regioselective Functionalization of Guanine:  First Practical Synthesis of Acyclic N9- and/or N7-Guanine Nucleosides Starting from N2,N9-Diacetylguanine The Journal of Organic Chemistry 1999
Regioselectivity and mechanism of transpurination reactions in the guanine nucleosides series Journal of the Chemical Society, Perkin Transactions 2 1997

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