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MRUKYOQQKHNMFI-PSQAKQOGSA-N

Compound with spectra: 1 NMR

MRUKYOQQKHNMFI-PSQAKQOGSA-N
SpectraBase Compound ID Az8KpfZRqNi
InChI InChI=1S/C9H11N5O5/c10-13-12-6-7(17)4(3-15)19-8(6)14-2-1-5(16)11-9(14)18/h1-2,4,6-8,15,17H,3H2,(H,11,16,18)/t4-,6-,7-,8-/m0/s1
InChIKey MRUKYOQQKHNMFI-PSQAKQOGSA-N
Mol Weight 269.22 g/mol
Molecular Formula C9H11N5O5
Exact Mass 269.076018 g/mol
Enantiomer InChIKey MRUKYOQQKHNMFI-XVFCMESISA-N

View Spectrum of MRUKYOQQKHNMFI-PSQAKQOGSA-N

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
DYFZTUHXHLQLAT-BQUFFADESA-N
5'-S-(4-METHOXYPHENYL)-5'-THIOURIDINE
5'-[3''-(PHENYLIDEN)-CARBAZOYL]-URIDINE
5'-S-(4-HYDROXYPHENYL)-5'-THIOURIDINE
Uridine, 5-iodo-
5-Iodouridine
1-(3,5-Anhydro-2-O-methyl-.beta.,D-xylofuranosyl)uracil
5-FLUORO-1-BETA-D-ARABINOFURANOSYL-URACIL
1-[6(E)-TRIBUTYLSTANNYL-5,6-DIDEOXY-BETA-D-RIBO-HEX-5-ENOFURANOSYL]URACIL
5-CHLOROURIDINE
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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