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#10;2-[(1-TERT.-BUTYLDIMETHYLSILOXY-2,2,2-TRIFLUORO-1-TRIFLUOROMETHYL)-ETHYL]-PHENYL-(3,3,3-TRIFLUORO-2-HYDROXY-1-PHENYL-2-TRIFLUOROMETHYL)-PROPYL-SULFIDE

Compound with spectra: 2 NMR

#10;2-[(1-TERT.-BUTYLDIMETHYLSILOXY-2,2,2-TRIFLUORO-1-TRIFLUOROMETHYL)-ETHYL]-PHENYL-(3,3,3-TRIFLUORO-2-HYDROXY-1-PHENYL-2-TRIFLUOROMETHYL)-PROPYL-SULFIDE
SpectraBase Compound ID JR6OvHn4L8u
InChI InChI=1S/C25H26F12O2SSi/c1-19(2,3)41(4,5)39-21(24(32,33)34,25(35,36)37)16-13-9-10-14-17(16)40-18(15-11-7-6-8-12-15)20(38,22(26,27)28)23(29,30)31/h6-14,18,38H,1-5H3
InChIKey MNNCVMGOQXUNOU-UHFFFAOYSA-N
Mol Weight 646.61 g/mol
Molecular Formula C25H26F12O2SSi
Exact Mass 646.123116 g/mol

View Spectrum of #10;2-[(1-TERT.-BUTYLDIMETHYLSILOXY-2,2,2-TRIFLUORO-1-TRIFLUOROMETHYL)-ETHYL]-PHENYL-(3,3,3-TRIFLUORO-2-HYDROXY-1-PHENYL-2-TRIFLUOROMETHYL)-PROPYL-SULFIDE

19F NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3

View Spectrum of #10;2-[(1-TERT.-BUTYLDIMETHYLSILOXY-2,2,2-TRIFLUORO-1-TRIFLUOROMETHYL)-ETHYL]-PHENYL-(3,3,3-TRIFLUORO-2-HYDROXY-1-PHENYL-2-TRIFLUOROMETHYL)-PROPYL-SULFIDE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
VHXCJHQWXMIYNC-VQTJNVASSA-N
VHXCJHQWXMIYNC-PMACEKPBSA-N
3H-2,1-Benzoxathiole, 1,1-dihydro-5-methyl-3,3-bis(trifluoromethyl)-1,1-bis[2,2,2-trifluoro -1-phenyl-1-(trifluoromethyl)ethoxy]-
4-quinolinecarboxylic acid, 2-(4-methoxyphenyl)-, 2-(4-chloro-3-nitrophenyl)-2-oxoethyl ester
(S)-2-[2-(4-Chloro-phenyl)-2,3-dihydro-benzo[b][1,4]thiazepin-4-yl]-3,5-dimethoxy-phenol
4-tert-Butyl-2,2,6,6-tetrakis(trifluoromethyl)-8-/.lambda.-4/-(1,2)oxathiolo(4,3,2-hi)(2,1)benzoxathiol anion
cis-2,4,5-triphenyl-5-trifluoromethyl-3-oxazoline
2-[N-Formyl-N-(2-(N,N-diethylamido)phenyl)amino]-1-tosyl-8-[3,4-(methylenedioxy)phenyl]octene
trans-Bis(6,6,9,9-Tetramethy-5,6,7,8,8a,9,10,10a-octahydroacridin-2-yl) ether
9-trimethylsiloxy-10-methylthio-9,10-dihydrophenanthrene
Title Journal or Book Year
Synthesis, Crystal Structure, and Thermolysis of a Pentacoordinate 1,2λ6-Oxathietane:  An Intermediate of the Corey−Chaykovsky Reaction of Oxosulfonium Ylides? Journal of the American Chemical Society 1996
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