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(1S,2R,3S,4S,6S)-4-(ACETOXYMETHYL)-6-[4-(4-FLUOROPHENYL)-1H-1,2,3-TRIAZOL-1-YL]-4-HYDROXY-CYCLOHEXANE-1,2,3-TRIYL-TRIACETATE

Compound with spectra: 1 NMR

(1S,2R,3S,4S,6S)-4-(ACETOXYMETHYL)-6-[4-(4-FLUOROPHENYL)-1H-1,2,3-TRIAZOL-1-YL]-4-HYDROXY-CYCLOHEXANE-1,2,3-TRIYL-TRIACETATE
SpectraBase Compound ID XaLzIE0UA8
InChI InChI=1S/C23H26FN3O9/c1-12(28)33-11-23(32)9-19(27-10-18(25-26-27)16-5-7-17(24)8-6-16)20(34-13(2)29)21(35-14(3)30)22(23)36-15(4)31/h5-8,10,19-22,32H,9,11H2,1-4H3/t19-,20-,21+,22-,23-/m0/s1
InChIKey PTISQFDKTOUIBE-HPAIXVDQSA-N
Mol Weight 507.47 g/mol
Molecular Formula C23H26FN3O9
Exact Mass 507.165308 g/mol
Enantiomer InChIKey PTISQFDKTOUIBE-XNBWIAOKSA-N

View Spectrum of (1S,2R,3S,4S,6S)-4-(ACETOXYMETHYL)-6-[4-(4-FLUOROPHENYL)-1H-1,2,3-TRIAZOL-1-YL]-4-HYDROXY-CYCLOHEXANE-1,2,3-TRIYL-TRIACETATE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(1S,2R,3S,4S,6S)-4-(ACETOXYMETHYL)-4-HYDROXY-6-[4-(4-METHOXYPHENYL)-1H-1,2,3-TRIAZOL-1-YL]-CYCLOHEXANE-1,2,3-TRIYL-TRIACETATE
(1S,2R,3S,4S,6S)-4-(Acetoxymethyl)-4-hydroxy-6-[4-(4-methylphenyl)-1H-1,2,3-triazol-1-yl]cyclohexane-1,2,3-triyl Triacetate
(1S,2R,3S,4S,6S)-4-(ACETOXYMETHYL)-6-[4-(4-CHLOROPHENYL)-1H-1,2,3-TRIAZOL-1-YL]-4-HYDROXY-CYCLOHEXANE-1,2,3-TRIYL-TRIACETATE
(1S,2R,3S,4S,6S)-4-(ACETOXYMETHYL)-4-HYDROXY-6-(4-PHENYL-1H-1,2,3-TRIAZOL-1-YL)-CYCLOHEXANE-1,2,3-TRIYL-TRIACETATE
(1S,2R,3S,4S,6S)-4-(ACETOXYMETHYL)-6-(4-BUTYL-1H-1,2,3-TRIAZOL-1-YL)-4-HYDROXY-CYCLOHEXANE-1,2,3-TRIYL-TRIACETATE
(1S,2R,3S,4S,6S)-4-(ACETOXYMETHYL)-4-HYDROXY-6-[4-(PHENOXYMETHYL)-1H-1,2,3-TRIAZOL-1-YL]-CYCLOHEXANE-1,2,3-TRIYL-TRIACETATE
(+/-)-OXYMITRONE
12.beta.-(ethoxyethoxy)picrasan-3.beta.-ol
(S)-N-(3,7,8,9-Tetrahydro-2-hydroxy-4,11,12,13-tetramethoxy-3-oxocyclohepta[a][3]benzoxocin-7-yl)aceramide
1.alpha.-Acetoxy-5-carbomethoxy-10a.alpha.-hydroxy-8-oxo-1,2,10a.alpha.,10b.alpha.-tetrahydro-4H-3a-azabenz[e]azulen-3,8-dione
Title Journal or Book Year
Synthesis of 1,2,3-Triazoles from Azide-Derivatised Aminocyclitols by Catalytic Diazo Transfer and CuAAC Click Chemistry European Journal of Organic Chemistry 2014
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