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5'-O-(TERT.-BUTYLDIMETHYLSILYL)-2'-CHLORO-2'-DEOXYADENOSINE

Compound with spectra: 1 NMR

5'-O-(TERT.-BUTYLDIMETHYLSILYL)-2'-CHLORO-2'-DEOXYADENOSINE
SpectraBase Compound ID HR7uWWqIhnG
InChI InChI=1S/C16H26ClN5O3Si/c1-16(2,3)26(4,5)24-6-9-12(23)10(17)15(25-9)22-8-21-11-13(18)19-7-20-14(11)22/h7-10,12,15,23H,6H2,1-5H3,(H2,18,19,20)/t9-,10-,12-,15-/m0/s1
InChIKey CEKNSILIQOUOHE-OUCVZQCGSA-N
Mol Weight 399.95 g/mol
Molecular Formula C16H26ClN5O3Si
Exact Mass 399.149344 g/mol
Enantiomer InChIKey CEKNSILIQOUOHE-NDLNZWKESA-N

View Spectrum of 5'-O-(TERT.-BUTYLDIMETHYLSILYL)-2'-CHLORO-2'-DEOXYADENOSINE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent DMSO-D6
5'-O-(TERT.-BUTYLDIMETHYLSILYL)-2'-DEOXY-2'-FLUOROADENOSINE
9-[5-O-(TERT.-BUTYLDIMETHYLSILYL)-2-DEOXY-2-FLUORO-BETA-D-ARABINOFURANOSYL]-ADENINE
5'-O-(TERT.-BUTYLDIMETHYLSILYL)-2',3'-DIDEOXY-3'-(R/S)-DEUTERIO-2'-FLUOROADENOSINE
RMIAANGDAQJRIT-GTBBIVDNSA-N
ADENOSINE-5'-METHYLTHIOLPHOSPHATE
Adenosine, 5'-(tetramethylphosphorodiamidate)
5'-O-[5-[(TOL-4-YL)-SULFONYLOXY]-PENTYL]-ADENOSINE
9-[5-O-(TERT.-BUTYLDIMETHYLSILYL)-2,3-DIDEOXY-2-(R/S)-DEUTERIO-3-FLUORO-BETA-D-THREO-PENTOFURANOSYL]-ADENINE
5'-O-CARBAZOYLADENOSINE
5'-O-Butyryl-adenosine
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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