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(4RS,4ASR,10BRS)-4A,10B-DIHYDRO-2-METHYL-4-PHENYL-1-PHENYLSULFENYL-4H,5H-PYRANO-[3,4-C]-[1]-BENZOPYRAN

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

(4RS,4ASR,10BRS)-4A,10B-DIHYDRO-2-METHYL-4-PHENYL-1-PHENYLSULFENYL-4H,5H-PYRANO-[3,4-C]-[1]-BENZOPYRAN
SpectraBase Compound ID DCUPUwDJxAH
InChI InChI=1S/C25H22O2S/c1-17-25(28-19-12-6-3-7-13-19)23-20-14-8-9-15-22(20)26-16-21(23)24(27-17)18-10-4-2-5-11-18/h2-15,21,23-24H,16H2,1H3/t21-,23+,24+/m0/s1
InChIKey VMTLPKZNLFSFMD-QPTUXGOLSA-N
Mol Weight 386.51 g/mol
Molecular Formula C25H22O2S
Exact Mass 386.134051 g/mol
Enantiomer InChIKey VMTLPKZNLFSFMD-NHTMILBNSA-N

View Spectrum of (4RS,4ASR,10BRS)-4A,10B-DIHYDRO-2-METHYL-4-PHENYL-1-PHENYLSULFENYL-4H,5H-PYRANO-[3,4-C]-[1]-BENZOPYRAN

MS (GC) Spectrum
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Source of Spectrum AH-132-400-16

View Spectrum of (4RS,4ASR,10BRS)-4A,10B-DIHYDRO-2-METHYL-4-PHENYL-1-PHENYLSULFENYL-4H,5H-PYRANO-[3,4-C]-[1]-BENZOPYRAN

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
  • (4S,4aR,10bS)-2-methyl-4-phenyl-1-(phenylthio)-4,4a,5,10b-tetrahydropyrano[3,4-c]chromene
3-(m-Bromobenzoyloxy)-7-[4-Methyl-6-[(2,5-dimethoxy-3-methyl)phenyl]-2-(hydroxy)hex-4-en-1-yl]-6,7,9,9-tetramethylbicyclo[4.2.1]nonane-2-ol
TMS-7.alpha.,11-di-OH-methyl-8-tetrahydrocannabinol
1-(1-Hydroxy-6,6-dimethyl-6a,12b-dihydro-6H,7H-5,8-dioxabenzo[c]phenanthrene-2-yl)propane-1-one
a2-(5-Hydroxybenzofuran-3-yl)-3-methylthiazolo[3,2-a]benzimidazole
ENDO-9-TERT.-BUTYL-1,2,3,4-TETRAHYDRO-N-(4-METHOXYPHENYL)-1,4-IMINONAPHTHALIN-2,3-DICARBOXIMIDE
1-[(4R,5R,6S)-5-Acetyl-4-hydroxy-4-methyl-6-(3-nitro-phenyl)-2-phenylamino-cyclohex-1-enyl]-ethanone
(R)-5-fluoro-3-((R)-2-nitro-1-(4-(trifluoromethyl)phenyl)ethyl)-3-phenylindolin-2-one
1-Ethyl-4-keto-5,8-dimethoxy-6-nitro-quinoline-3-carboxylic acid
6-amino-4-(3,4-dichlorophenyl)-3-(3-methoxyphenyl)-1,4-dihydropyrano[2,3-c]pyrazole-5-carbonitrile
15-ISOPROPYL-3-METHOXY-ESTRA-1,3,5(10),15-TETRAEN-17-ONE
Title Journal or Book Year
Polycyclic 2H-Pyran Derivatives by Intramolecular Hetero-Diels-Alder Reactionsof a-Sulfur-Substituted a,b-UnsaturatedCarbonyl Compounds Monatshefte fuer Chemie/Chemical Monthly 2001
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