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IFVJLCHSLGMHEY-CIXYTLPCSA-N

Compound with spectra: 1 NMR

IFVJLCHSLGMHEY-CIXYTLPCSA-N
SpectraBase Compound ID JBizYCFjCKt
InChI InChI=1S/C10H12N8O3/c11-8-6-9(14-2-13-8)18(3-15-6)10-5(16-17-12)7(20)4(1-19)21-10/h2-5,7,10,19-20H,1H2,(H2,11,13,14)/t4-,5-,7-,10-/m0/s1
InChIKey IFVJLCHSLGMHEY-CIXYTLPCSA-N
Mol Weight 292.26 g/mol
Molecular Formula C10H12N8O3
Exact Mass 292.103236 g/mol
Enantiomer InChIKey IFVJLCHSLGMHEY-QYYRPYCUSA-N

View Spectrum of IFVJLCHSLGMHEY-CIXYTLPCSA-N

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
(2S,3R,4R,5S)-5-(6-aminopurin-9-yl)-4-azido-2-methylol-tetrahydrofuran-3-ol
CORDYSININ_B
Adenosine, 2'-O-methyl-
2'-O-methyl-adenosine
Adenosine, 2'-O-propyl-
Adenosine, 5'-(tetramethylphosphorodiamidate)
ADENOSINE, 5'-METHYLPHOSPHATE
HROXHMRQKGGIFT-ROXUDPPMSA-M
9β-D-Arabinofuranosyladenine-5'-monophosphate
Adenosine-5'-monophosphate dianion
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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