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[1-[5-METHYL-4,7,12-TRIOXO-11-(PENTANOYLOXY)-7,12-DIHYDRO-4H-NAPHTHO-[2,3-H]-CHROMEN-2-YL]-ETHYL]-TRIPHENYLPHOSPHONIUM-BROMIDE

Compound with spectra: 1 NMR

[1-[5-METHYL-4,7,12-TRIOXO-11-(PENTANOYLOXY)-7,12-DIHYDRO-4H-NAPHTHO-[2,3-H]-CHROMEN-2-YL]-ETHYL]-TRIPHENYLPHOSPHONIUM-BROMIDE
SpectraBase Compound ID Lj7phGRkcHh
InChI InChI=1S/2C43H36O6P.2BrH/c2*1-4-5-24-37(45)48-35-23-15-22-32-39(35)42(47)40-33(41(32)46)25-27(2)38-34(44)26-36(49-43(38)40)28(3)50(29-16-9-6-10-17-29,30-18-11-7-12-19-30)31-20-13-8-14-21-31;;/h2*6-23,25-26,28H,4-5,24H2,1-3H3;2*1H/q2*+1;;/p-2
InChIKey CARHJBGZHDTGDR-UHFFFAOYSA-L
Mol Weight 1519.266 g/mol
Molecular Formula C86H72Br2O12P2
Exact Mass 1516.286578 g/mol
Parent InChIKey IRSAKEUXLJSDQM-UHFFFAOYSA-M

View Spectrum of [1-[5-METHYL-4,7,12-TRIOXO-11-(PENTANOYLOXY)-7,12-DIHYDRO-4H-NAPHTHO-[2,3-H]-CHROMEN-2-YL]-ETHYL]-TRIPHENYLPHOSPHONIUM-BROMIDE

13C NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
Title Journal or Book Year
General Approach to Anthrapyran Antibiotics Exemplified by the Synthesis of rac-γ-Indomycinone European Journal of Organic Chemistry 2011
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