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4-[(DICYCLOHEXYLTHIOOXOPHOSPHORANYL)-(ETHOXYCARBONYL)-METHYL]-5-ETHOXY-2,3-FURAN-DICARBOXYLIC-ACID-METHYLESTER

Compound with spectra: 1 NMR

4-[(DICYCLOHEXYLTHIOOXOPHOSPHORANYL)-(ETHOXYCARBONYL)-METHYL]-5-ETHOXY-2,3-FURAN-DICARBOXYLIC-ACID-METHYLESTER
SpectraBase Compound ID JZ8PWqjd0B7
InChI InChI=1S/C28H43O8PS/c1-5-32-25(29)21-22(28(35-8-4)36-23(21)26(30)33-6-2)24(27(31)34-7-3)37(38,19-15-11-9-12-16-19)20-17-13-10-14-18-20/h19-20,24H,5-18H2,1-4H3
InChIKey ZIZWQSJDMMTILO-UHFFFAOYSA-N
Mol Weight 570.7 g/mol
Molecular Formula C28H43O8PS
Exact Mass 570.241627 g/mol

View Spectrum of 4-[(DICYCLOHEXYLTHIOOXOPHOSPHORANYL)-(ETHOXYCARBONYL)-METHYL]-5-ETHOXY-2,3-FURAN-DICARBOXYLIC-ACID-METHYLESTER

31P NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
#15;(2R,3R,4S,5R,6R)-2-(ACETOXYMETHYL)-6-[4-[[(2R,3S,5R)-2-(AZIDOMETHYL)-5-(5-METHYL-2,4-DIOXO-3,4-DIHYDRO-PYRIMIDIN-1(2H)-YL]-TETRAHYDROFURAN-3-YL-OXY]-METHYL
allyl (2Z)-7-methyl-2-{[5-(3-nitrophenyl)-2-furyl]methylene}-3-oxo-5-phenyl-2,3-dihydro-5H-[1,3]thiazolo[3,2-a]pyrimidine-6-carboxylate
DELPHINIDIN-3,7,3',5'-TETRA-O-(6-O-PARA-COUMAROYL-BETA-GLUCOPYRANOSIDE)
2H-cyclopenta[4,5]thieno[2,3-d]pyrimidine-1-acetamide, 1,3,4,5,6,7-hexahydro-2,4-dioxo-3-phenyl-N-[(tetrahydro-2-furanyl)methyl]-
1,2-Dihydroxy-7H-dibenzo[de,g]quinolin-7-one
UYVJUSXEGXNRGE-UHFFFAOYSA-N
6-Chloro-2-(N'-methyl-2'-pyrrolyl)-9.beta.-(2',3',5'-tri-O-acetyl)-D,ribo-furanosylpurine
LFOFQKPNSBQLFJ-UHFFFAOYSA-N
7-Methyl-10-thioxo-9,10,11,12-tetrahydrochromeno[4',3':4,5]pyrido[2,3-d]pyrimidine-6,12-dione
4,7,10-tribromo-1-methoxy-7,8,9,10-tetrahydronaphtho[1,2-c]isochromen-6-one
Title Journal or Book Year
Darstellung und Eigenschaften von und Reaktionen mit metallhaltigen Heterocyclen, LXIX 1 ) Unabhängige Mechanismen der Cyclocotrimerisierung von Thiophosphinitomangan‐Komplexen mit Alkinen. – Ein einfacher Zugang zu fünfgliedrigen Heterocyclen Chemische Berichte 1990
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