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XOTUXDQKWDTKSI-PSQAKQOGSA-N

Compound with spectra: 1 NMR

XOTUXDQKWDTKSI-PSQAKQOGSA-N
SpectraBase Compound ID HoTzNexlBiE
InChI InChI=1S/C9H11ClN2O5/c10-6-7(15)4(3-13)17-8(6)12-2-1-5(14)11-9(12)16/h1-2,4,6-8,13,15H,3H2,(H,11,14,16)/t4-,6-,7-,8-/m0/s1
InChIKey XOTUXDQKWDTKSI-PSQAKQOGSA-N
Mol Weight 262.65 g/mol
Molecular Formula C9H11ClN2O5
Exact Mass 262.035649 g/mol
Enantiomer InChIKey XOTUXDQKWDTKSI-XVFCMESISA-N

View Spectrum of XOTUXDQKWDTKSI-PSQAKQOGSA-N

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
1-(3-Chloro-4-hydroxy-5-methylol-tetrahydrofuran-2-yl)pyrimidine-2,4-quinone
FEUDNSHXOOLCEY-PSQAKQOGSA-N
KVQOKCWRUQHGQR-PSQAKQOGSA-N
1-ß-D-Arabinofuranosyluracil
1-[(2S,3S,4S,5S)-3-fluoro-4-hydroxy-5-methylol-tetrahydrofuran-2-yl]pyrimidine-2,4-quinone
1-[5-(chloromethyl)-3,4-bis(oxidanyl)oxolan-2-yl]pyrimidine-2,4-dione
[4-17O]-URIDINE
2,4(1H,3H)-Pyrimidinedione, 1-(3-chloro-3-deoxy-.beta.-D-xylofuranosyl)-
[2-17O]-URIDINE
3,4-dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl)-2-thioxo-2,3-dihydropyrimidin-4(1H)-one
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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