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DYFZTUHXHLQLAT-BQUFFADESA-N

Compound with spectra: 1 NMR

DYFZTUHXHLQLAT-BQUFFADESA-N
SpectraBase Compound ID K5TTN3eYhqS
InChI InChI=1S/C15H25FN2O5Si/c1-15(2,3)24(4,5)22-8-9-12(20)11(16)13(23-9)18-7-6-10(19)17-14(18)21/h6-7,9,11-13,20H,8H2,1-5H3,(H,17,19,21)/t9-,11-,12-,13-/m0/s1
InChIKey DYFZTUHXHLQLAT-BQUFFADESA-N
Mol Weight 360.46 g/mol
Molecular Formula C15H25FN2O5Si
Exact Mass 360.151677 g/mol
Enantiomer InChIKey DYFZTUHXHLQLAT-OJAKKHQRSA-N

View Spectrum of DYFZTUHXHLQLAT-BQUFFADESA-N

19F NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
URIDINE-5'-MONOPHOSPHOROTHIOATE
5'-O-Butyrylarauridine
1-Uracil-5-ribofuranosyl Butanoate
TYXCUKNZAWEEGG-BVALORAHSA-N
5'-O-Butyryl-uridine
5'-[3''-(PROPYLIDEN)-CARBAZOYL]-URIDINE
GWUYRXBKXOURDF-XDYITYJNSA-N
5'-O-(VINYLOXY)-CARBONYLURIDINE
1-uracil-5-ribofuranosyl Decanoate
WFGZGVFNINQBOW-MGHWNKPDSA-N
Title Journal or Book Year
Nucleic Acid Related Compounds. 91. Biomimetic Reactions Are in Harmony with Loss of 2‘-Substituents as Free Radicals (Not Anions) during Mechanism-Based Inactivation of Ribonucleotide Reductases. Differential Interactions of Azide, Halogen, and Alkylthio Groups with Tributylstannane and Triphenylsilane1 Journal of the American Chemical Society 1996

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