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(S)-4,8-DI-TERT.-BUTYL-6-IODO-1,2,10,11-TETRAMETHYL-5,7-DIOXA-6-PHOSPHA-DIBENZO-[A,C]-CYCLOHEPTENE

Compound with spectra: 2 NMR

(S)-4,8-DI-TERT.-BUTYL-6-IODO-1,2,10,11-TETRAMETHYL-5,7-DIOXA-6-PHOSPHA-DIBENZO-[A,C]-CYCLOHEPTENE
SpectraBase Compound ID DD9W5qjNL1s
InChI InChI=1S/C24H32IO2P/c1-13-11-17(23(5,6)7)21-19(15(13)3)20-16(4)14(2)12-18(24(8,9)10)22(20)27-28(25)26-21/h11-12H,1-10H3
InChIKey IQZFOLBLGBKZBZ-UHFFFAOYSA-N
Mol Weight 510.4 g/mol
Molecular Formula C24H32IO2P
Exact Mass 510.118462 g/mol

View Spectrum of (S)-4,8-DI-TERT.-BUTYL-6-IODO-1,2,10,11-TETRAMETHYL-5,7-DIOXA-6-PHOSPHA-DIBENZO-[A,C]-CYCLOHEPTENE

31P NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C6D6

View Spectrum of (S)-4,8-DI-TERT.-BUTYL-6-IODO-1,2,10,11-TETRAMETHYL-5,7-DIOXA-6-PHOSPHA-DIBENZO-[A,C]-CYCLOHEPTENE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C6D6
(S)-4,8-DI-TERT.-BUTYL-6-BROMO-1,2,10,11-TETRAMETHYL-5,7-DIOXA-6-PHOSPHA-DIBENZO-[A,C]-CYCLOHEPTENE
(S)-4,8-BIS-(1,1-DIMETHYLETHYL)-1,2,10,11-TETRAMETHYL-6-PHENOXY-DIBENZO-[D,F]-(1,3,2)-DIOXAPHOSPHEPIN
(S)-4,8-DI-TERT.-BUTYL-6-CHLORO-1,2,10,11-TETRAMETHYL-5,7-DIOXA-6-PHOSPHA-DIBENZO-[A,C]-CYCLOHEPTENE
N-(2,4,8,10-tetra-tert-butyldiphenyl[d,f]{1,3,2}dioxaphosphazin-6-yl)maleimide
N-(2,4,8,10-tetra-tert-butyldiphenyl[d,f]{1,3,2}dioxaphosphazin-6-yl)-N,N'-dimethylurea
N-(2,4,8,10-Tetra-tert-butyl-dibenz[d,f]{1,3,2}dioxaphosphepin-6-yl)-N-methylaniline
3,3'-BIS-(1,1-DIMETHYLETHYL)-2,2'-[[3,3',5,5'-TETRAKIS-(1,1-DIMETHYLETHYL)-1,1'-BIPHENYL-2,2'-DIYL]-BIS-(OXY)]-BIS-[1,3,2-OXAZAPHOSPHOLIDINE]
3,4-Benzo-7-(.beta.-bromoallyloxy)-8-methylcoumarin
4-methyl-3-[(3-methyl-2-butenyl)oxy]-6H-benzo[c]chromen-6-one
(R,R)-[4,8-BIS-(2-METHYLALLYL)-5,7-DIOXA-6-PHOSPHADIBENZO-[A,C]-CYCLOHEPTEN-6-YL]-BIS-(1-PHENYLPROPYL)-AMINE
Title Journal or Book Year
Synthesis and Application of a New Bisphosphite Ligand Collection for Asymmetric Hydroformylation of Allyl Cyanide The Journal of Organic Chemistry 2004
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