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49902
Zinn(II)-Ionophor I
Selectophore™
Synonym(e):
Dibenzo-18-Krone-6, 2,3,11,12-Dibenzo-1,4,7,10,13,16-hexaoxacyclooctadeca-2,11-dien, 6,7,9,10,17,18,20,21-Octahydrodibenzo[b,k][1,4,7,10,13,16]hexaoxacyclooctadecen, DB18C6
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Über diesen Artikel
Empirische Formel (Hill-System):
C20H24O6
CAS-Nummer:
Molekulargewicht:
360.40
EC Number:
238-041-3
UNSPSC Code:
26111700
PubChem Substance ID:
Beilstein/REAXYS Number:
1162153
MDL number:
product line
Selectophore™
mp
162-164 °C (lit.)
SMILES string
C1COc2ccccc2OCCOCCOc3ccccc3OCCO1
InChI
1S/C20H24O6/c1-2-6-18-17(5-1)23-13-9-21-11-15-25-19-7-3-4-8-20(19)26-16-12-22-10-14-24-18/h1-8H,9-16H2
InChI key
YSSSPARMOAYJTE-UHFFFAOYSA-N
General description
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Packaging
Bottomless glass bottle. Contents are inside inserted fused cone.
Legal Information
Selectophore is a trademark of Merck KGaA, Darmstadt, Germany
Lagerklasse
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
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A Carabez et al.
Biochimica et biophysica acta, 638(1), 125-131 (1981-11-12)
In rat liver mitochondria, the macrocyclic polyether, dibenzo-18-crown-6 (polyether XXVIII) inhibits the oxidation of NAD-dependent substrates, as stimulated by ADP, uncouplers and valinomycin plus K+. It does not inhibit the oxidation of succinate. It is concluded that polyether XXVIII inhibits
Jaroslav Kríz et al.
The journal of physical chemistry. A, 112(41), 10236-10243 (2008-09-25)
Interaction of dibenzo-18-crown-6 (DBC) with H 3O (+) (HP) in nitrobenzene- d 5 and dichloromethane- d 2 was studied by using (1)H and (13)C NMR spectra and relaxations, FTIR spectra, and quantum chemical DFT calculations. NMR shows that the DBC*HP
Marc Vidal et al.
Chemical communications (Cambridge, England), 47(48), 12834-12836 (2011-11-03)
We describe the synthesis of a diphenylglycoluril/dibenzo-crown-6 molecular chalice, the self-assembly at the air/water interface and its complexation properties in solution and at the water/chloroform interface.