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(1S,2R,3S,4S,6S)-4-(Acetoxymethyl)-4-hydroxy-6-[4-(4-nitrophenyl)-1H-1,2,3-triazol-1-yl]cyclohexane-1,2,3-triyl Triacetate

Compound with spectra: 1 NMR, and 1 MS (GC)

(1S,2R,3S,4S,6S)-4-(Acetoxymethyl)-4-hydroxy-6-[4-(4-nitrophenyl)-1H-1,2,3-triazol-1-yl]cyclohexane-1,2,3-triyl Triacetate
SpectraBase Compound ID BAg4NEaTVXJ
InChI InChI=1S/C23H26N4O11/c1-12(28)35-11-23(32)9-19(20(36-13(2)29)21(37-14(3)30)22(23)38-15(4)31)26-10-18(24-25-26)16-5-7-17(8-6-16)27(33)34/h5-8,10,19-22,32H,9,11H2,1-4H3/t19-,20-,21+,22-,23-/m0/s1
InChIKey GFSFQZQJGHMUFM-HPAIXVDQSA-N
Mol Weight 534.48 g/mol
Molecular Formula C23H26N4O11
Exact Mass 534.159808 g/mol
Enantiomer InChIKey GFSFQZQJGHMUFM-XNBWIAOKSA-N

View Spectrum of (1S,2R,3S,4S,6S)-4-(Acetoxymethyl)-4-hydroxy-6-[4-(4-nitrophenyl)-1H-1,2,3-triazol-1-yl]cyclohexane-1,2,3-triyl Triacetate

MS (GC) Spectrum
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Source of Spectrum U1-2014-3734-15f

View Spectrum of (1S,2R,3S,4S,6S)-4-(Acetoxymethyl)-4-hydroxy-6-[4-(4-nitrophenyl)-1H-1,2,3-triazol-1-yl]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 DMSO-D6
(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)-6-[4-(4-FLUOROPHENYL)-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
#15;(2R,3R,4S,5R,6R)-2-(ACETOXYMETHYL)-6-[4-[[(2R,3S,5R)-2-(AZIDOMETHYL)-5-(5-METHYL-2,4-DIOXO-3,4-DIHYDRO-PYRIMIDIN-1(2H)-YL]-TETRAHYDROFURAN-3-YL-OXY]-METHYL
(+/-)-OXYMITRONE
N-(2-(1'-benzyl-3'-(2''-ketocyclohexyl)oxindol-3'-yl)ethyl)-N-methylacetamide(diastereoisomer b)
ATHROLIDE_A;(1-S,2-S,4-R,5-S,6-S,7-R,8-S,10-R)-2-(2-METHYLPROPANOYLOXY)-4-ACETOXY-6-ACETOXYGUAI-11-(13)-EN-8,12-OLIDE
(S)-N-(3,7,8,9-Tetrahydro-2-hydroxy-4,11,12,13-tetramethoxy-3-oxocyclohepta[a][3]benzoxocin-7-yl)aceramide
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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