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ZRXKBYOZGUWWRN-RYVZHVEOSA-N

Compound with spectra: 1 NMR

ZRXKBYOZGUWWRN-RYVZHVEOSA-N
SpectraBase Compound ID LHFRsWItrlf
InChI InChI=1S/C11H15N5O6S/c1-23(19,20)22-8-7(18)5(2-17)21-11(8)16-4-15-6-9(12)13-3-14-10(6)16/h3-5,7-8,11,17-18H,2H2,1H3,(H2,12,13,14)/t5-,7-,8-,11-/m0/s1
InChIKey ZRXKBYOZGUWWRN-RYVZHVEOSA-N
Mol Weight 345.33 g/mol
Molecular Formula C11H15N5O6S
Exact Mass 345.074304 g/mol
Enantiomer InChIKey ZRXKBYOZGUWWRN-IOSLPCCCSA-N

View Spectrum of ZRXKBYOZGUWWRN-RYVZHVEOSA-N

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
2'-AMP;ADENOSINE-2'-MONOPHOSPHATE;REFERENCE-17
Adenosine 2'-phosphate
3'-O-LEVULINYL-2'-O-METHYLADENOSINE
ADENOSINE-5'-PHOSPHOROPYRAZOLIDE
3'-AMINO-3'-DESOXYADENOSINE-2'-THIONOPHOSPHATE
3'-Amino-3'-deoxyadenosine-2'-thionophosphate dianion
5'-O-(1-O-PALMITOYL-SN-GLYCERO-3-PHOSPHORYL)-ADENOSINE
ADENOSINE-5'-PHOSPHORO-1,2,4-TRIAZOLIDE
(ALPHA,BETA:BETA,GAMMA-BIS-METHYLENE)-DIADENOSINE-TRIPHOSPHATE-TRISODIUM-SALT
ADENOSINE-5'-PHOSPHORO-4-AMINOPYRIDINIUM
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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