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(D)-1,2:4,5-DI-O-CYCLOHEXYLIDENE-3-[(2S,4R,5S)-3,4-DIMETHYL-5-PHENYL-2-SULFIDE-1,3,2-OXAZAPHOSPHOLIDINYL]-MYO-INOSITOL

Compound with spectra: 4 NMR

(D)-1,2:4,5-DI-O-CYCLOHEXYLIDENE-3-[(2S,4R,5S)-3,4-DIMETHYL-5-PHENYL-2-SULFIDE-1,3,2-OXAZAPHOSPHOLIDINYL]-MYO-INOSITOL
SpectraBase Compound ID 25e8lMjTQ3h
InChI InChI=1S/C28H40NO7PS/c1-18-21(19-12-6-3-7-13-19)35-37(38,29(18)2)36-26-24-22(31-27(33-24)14-8-4-9-15-27)20(30)23-25(26)34-28(32-23)16-10-5-11-17-28/h3,6-7,12-13,18,20-26,30H,4-5,8-11,14-17H2,1-2H3/t18-,20-,21-,22-,23+,24-,25-,26-,37?/m1/s1
InChIKey LXRKCPBDYNWEIJ-KMLYNKTBSA-N
Mol Weight 565.7 g/mol
Molecular Formula C28H40NO7PS
Exact Mass 565.226311 g/mol
Enantiomer InChIKey LXRKCPBDYNWEIJ-BXOUCOCJSA-N

View Spectrum of (D)-1,2:4,5-DI-O-CYCLOHEXYLIDENE-3-[(2S,4R,5S)-3,4-DIMETHYL-5-PHENYL-2-SULFIDE-1,3,2-OXAZAPHOSPHOLIDINYL]-MYO-INOSITOL

31P NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD

View Spectrum of (D)-1,2:4,5-DI-O-CYCLOHEXYLIDENE-3-[(2S,4R,5S)-3,4-DIMETHYL-5-PHENYL-2-SULFIDE-1,3,2-OXAZAPHOSPHOLIDINYL]-MYO-INOSITOL

31P NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CD3OD

View Spectrum of (D)-1,2:4,5-DI-O-CYCLOHEXYLIDENE-3-[(2S,4R,5S)-3,4-DIMETHYL-5-PHENYL-2-SULFIDE-1,3,2-OXAZAPHOSPHOLIDINYL]-MYO-INOSITOL

31P NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of (D)-1,2:4,5-DI-O-CYCLOHEXYLIDENE-3-[(2S,4R,5S)-3,4-DIMETHYL-5-PHENYL-2-SULFIDE-1,3,2-OXAZAPHOSPHOLIDINYL]-MYO-INOSITOL

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (D)-2,3:5,6-DI-O-CYCLOHEXYLIDENE-1-[(2S,4R,5S)-3,4-DIMETHYL-5-PHENYL-2-SULFIDE-1,3,2-OXAZAPHOSPHOLIDINYL]-MYO-INOSITOL
(D)-2,3:5,6-DI-O-CYCLOHEXYLIDENE-1-[(2S,4R,5S)-3,4-DIMETHYL-5-PHENYL-2-SULFIDE-1,3,2-OXAZAPHOSPHOLIDINYL]-MYO-INOSITOL
5,5-DIMETHYL-3-(2-METHYL-2-HYDROXYPROPYL)-2-[1,2,5,6-DI-O-ISOPROPYLIDENE-ALPHA-D-GLUCOFURANOSYLOXY]-2-THIO-1,3,2-OXAZAPHOSPHOLIDINE
BUOBXCNIMARUBG-ZQZFWOJRSA-N
6,2',6'-O-TRIACETYL-3-O-TRANS-PARA-COUMAROYLSUCROSE
4-O-(2-AZIDO-3,4,6-TRI-O-BENZYL-2-DEOXY-BETA-D-GLUCOPYRANOSYL)-2,3-O-ISOPROPYLIDENE-D-XYLO-HEXOS-5-ULOSE-DIMETHYL-ACETAL
FMOBHBNYUVUTCC-JJBUQPDOSA-M
6'-O-[(E)-SINAPOYL]-GARDOSIDE
pyrido[2,3-d]pyrimidin-4(1H)-one, 5-(difluoromethyl)-2-mercapto-1-(2-methoxyethyl)-7-(3-methoxyphenyl)-
(20R)- and (20S)-24-Nor-5.alpha.-cholan-12-one
3,6-ANHYDRO-2-DEOXY-4,5:7,8-DI-O-(1-METHYLETHYLIDENE)-3-[(N-BENZYLOXYCARBONYL)-AMINOMETHYL]-BETA-D-GULO-OCTANOIC-ACID
3,6-ANHYDRO-2-DEOXY-4,5:7,8-BIS-O-ISOPROPYLIDENE-3-[(N-BENZYLOXYCARBONYL)-AMINOMETHYL]-ALPHA-D-MANNO-OCTANOIC-ACID
Title Journal or Book Year
Stereochemistry at Phosphorus of the Reaction Catalyzed by myo-Inositol Monophosphatase Journal of Medicinal Chemistry 2002
(D)-2,3:5,6-DI-O-CYCLOHEXYLIDENE-1-[(2S,4R,5S)-3,4-DIMETHYL-5-PHENYL-2-SULFIDE-1,3,2-OXAZAPHOSPHOLIDINYL]-MYO-INOSITOL
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