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3-METHYL-2,2,2-TRIPHENYL-2-H-CYCLOHEPTA-[D]-[1.2-LAMBDA-(5)]-OXAPHOSPHOLE

Compound with spectra: 4 NMR

3-METHYL-2,2,2-TRIPHENYL-2-H-CYCLOHEPTA-[D]-[1.2-LAMBDA-(5)]-OXAPHOSPHOLE
SpectraBase Compound ID ESJwKjQfiv1
InChI InChI=1S/C27H23OP/c1-22-26-20-12-5-13-21-27(26)28-29(22,23-14-6-2-7-15-23,24-16-8-3-9-17-24)25-18-10-4-11-19-25/h2-21H,1H3
InChIKey PKZGMVTZUGBAKH-UHFFFAOYSA-N
Mol Weight 395.46 g/mol
Molecular Formula C27H24OP
Exact Mass 395.156477 g/mol

View Spectrum of 3-METHYL-2,2,2-TRIPHENYL-2-H-CYCLOHEPTA-[D]-[1.2-LAMBDA-(5)]-OXAPHOSPHOLE

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

View Spectrum of 3-METHYL-2,2,2-TRIPHENYL-2-H-CYCLOHEPTA-[D]-[1.2-LAMBDA-(5)]-OXAPHOSPHOLE

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

View Spectrum of 3-METHYL-2,2,2-TRIPHENYL-2-H-CYCLOHEPTA-[D]-[1.2-LAMBDA-(5)]-OXAPHOSPHOLE

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

View Spectrum of 3-METHYL-2,2,2-TRIPHENYL-2-H-CYCLOHEPTA-[D]-[1.2-LAMBDA-(5)]-OXAPHOSPHOLE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
HDIUQHWRMVBQBO-UHFFFAOYSA-N
9-(4-(tert-butyl)benzyl)-2-methyl-9H-benzo[d]imidazo[1,2-a]imidazol-1-ium bromide
3-Butyl-4-bromo-1-ethoxybenz[c-1,2]oxaphosphinine 1-oxide
KYBZLRIXRRGHON-UHFFFAOYSA-N
GYXZDOFHAMOBNN-UHFFFAOYSA-M
5,8-dimethyl-2,5-dihydro-3H-[1,2,4]triazino[5,6-b]indole-3-thione
1-(2-{[(1-ethyl-4-hydroxy-2-oxo-1,2-dihydro-3-quinolinyl)carbonyl]amino}ethyl)piperazinediium dichloride
N-dodecyl-1-ethyl-4-hydroxy-2-oxo-1,2-dihydro-3-quinolinecarboxamide
[RH-[1,2-BIS-[(2R,5R)-2,5-DIETHYLPHOSPHALANO]-BENZENE]]-TRIFLATE-WITH-LABELED-SUBSTRATE-7B;UNBOUND-SUBSTRATE
3,4-Benzo-2,2-diphenyl-1-rhenia-2-phospha-cyclopentane-1,1,1,1-tetracarbonyl
Title Journal or Book Year
Substituent effect on the transition from ionic to covalent bonding in triphenylphosphonium ylide derivatives: reactivity of 3-methyl-2,2,2-triphenyl-2H-cyclohepta[d][1,2λ5]oxaphosphole with heterocumulenes Journal of the Chemical Society, Perkin Transactions 2 2002
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