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OQMRMFRRRXIQFB-UHFFFAOYSA-N

Compound with spectra: 1 NMR

OQMRMFRRRXIQFB-UHFFFAOYSA-N
SpectraBase Compound ID 4ldDJJAmk7B
InChI InChI=1S/C10H17O4PS.4CO.Mn/c1-5-13-9(11)7-8(15(3,4)16)10(12)14-6-2;4*1-2;/h15H,5-6H2,1-4H3;;;;;/q-1;;;;;+1
InChIKey OQMRMFRRRXIQFB-UHFFFAOYSA-N
Mol Weight 431.25 g/mol
Molecular Formula C14H17MnO8PS
Exact Mass 430.976219 g/mol
Parent InChIKey NWGPYNKODGHHQY-UHFFFAOYSA-N

View Spectrum of OQMRMFRRRXIQFB-UHFFFAOYSA-N

31P NMR Spectrum
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent C6D6
(Tetradeuterio)clomipramine
1,3-dimethyl-4-(furfurylamino)-1H-pyrazolo[3,4-b]pyridine-5-carboxylic acid, ethyl ester
SOLIDAGOLACTONE V
9-Isopropyl-7,12-dimethylbenzo[d]heptalen-4-ol
6-CHLORONONAFLUORO-1,4-DIHYDRONAPHTHALENE
tert-Butyl (2R*,7aR*)-2-Azido-2-methyl-3-oxo-tetrahydro-1H-pyrrolizine-7a(5H)-carboylate
5,6-Dihydro-5,5-diphenylpyrano[2,3,4-de]chromen-2-one
IMLRHWGORMLZGL-GHRIWEEISA-N
N-Methyl-4-(2'-furyl)-3-acetyl-5-(ethoxycarbonyl)-2,6-dimethyl-1,4-dihydropyridine
(1RS,5RS,6RS,7SR)-5-hydroxy-7-isopropenyl-2,2,5-trimethylbicyclo[4.1.0]heptyl methyl ketone isomer A
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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