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(2R*,3S*,4S*,5R*,6R*,7S*)-1,8,9,10-TETRACHLORO-11,11-DIMETHOXYTRICYCLO-[6.2.1.0-(2,7)]-UNDEC-9-ENE-3,4,5,6-TETRAOL

Compound with spectra: 1 NMR

(2R*,3S*,4S*,5R*,6R*,7S*)-1,8,9,10-TETRACHLORO-11,11-DIMETHOXYTRICYCLO-[6.2.1.0-(2,7)]-UNDEC-9-ENE-3,4,5,6-TETRAOL
SpectraBase Compound ID ID1Yqulf9uI
InChI InChI=1S/C13H16Cl4O6/c1-22-13(23-2)11(16)3-4(12(13,17)10(15)9(11)14)6(19)8(21)7(20)5(3)18/h3-8,18-21H,1-2H3/t3-,4+,5+,6-,7+,8-,11-,12-/m1/s1
InChIKey XAVJTJNIXWZMOQ-SSZOUESESA-N
Mol Weight 410.1 g/mol
Molecular Formula C13H16Cl4O6
Exact Mass 407.970099 g/mol
Enantiomer InChIKey XAVJTJNIXWZMOQ-DESVVUSESA-N

View Spectrum of (2R*,3S*,4S*,5R*,6R*,7S*)-1,8,9,10-TETRACHLORO-11,11-DIMETHOXYTRICYCLO-[6.2.1.0-(2,7)]-UNDEC-9-ENE-3,4,5,6-TETRAOL

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
(2R*,3S*,4S*,5R*,6S*,7S*)-1,8,9,10-TETRACHLORO-11,11-DIMETHOXYTRICYCLO-[6.2.1.0-(2,7)]-UNDEC-9-ENE-3,4,5,6-TETRAOL
(+/-)-(1R*,2R*,3S*,6R*,7S*,8S*)-1,8,9,10-TETRACHLORO-11,11-DIMETHOXYTRICYCLO-[6.2.1.0(2,7)]-UNDEC-9-EN-3,6-DIOL
2,7:3,6-Dimethanonaphth[2,3-b]oxiren-8-ol, 3,4,5,6,9,9-hexachloro-1a,2,2a,3,6,6a,7,7a-octahydro-, stereoisomer
(1R*,4S*,7R*)-1,2,3,4,7-Pentachloro-7-methoxy-5-phenylbicyclo[2.2.1]hept-2-ene
No Name
endo/exo-3,4,5,6,12,12-Hexachloro-11-oxatetracyclo[6.2.1.1(3,6).0(2,7)]dodeca-4,9-diene
1,4:5,8-Dimethanonaphthalene-2,3-diol, 5,6,7,8,9,9-hexachloro-1,2,3,4,4a,5,8,8a-octahydro-, (1.alpha.,2.alpha.,3.beta.,4.alpha.,4a.beta.,5.alpha.,8.alpha.,8a.beta.)-
FRCCEHPWNOQAEU-GOTXYKCYSA-N
HEPTACHLOR;1-EXO-4,5,6,7,8,8-HEPTACHLORO-3,3A,4,7A-TETRAHYDRO-4,7-METHANO-1H-INDENE
6-N-ACETYL-6-N-ALLYL-2',3',5'-TRIS-O-(tert-BUTYL-DIMETHYLSILYL)-ADENOSINE
4H-pyrano[4',3':4,5]thieno[2,3-d]pyrimidin-4-one, 2-[[(3,4-dichlorophenyl)methyl]thio]-6-ethyl-3,5,6,8-tetrahydro-6-methyl-3-phenyl-
Title Journal or Book Year
Polycyclitols — Novel conduritol and carbasugar hybrids as new glycosidase inhibitors Canadian Journal of Chemistry 2005
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