Dibenzo-18-crown-6

Dibenzo-18-crown-6
Identifiers
CAS Number	14187-32-7 ;
3D model (JSmol)	Interactive image;
ChEBI	CHEBI:358732 ;
ChEMBL	ChEMBL345536 ;
ChemSpider	24722 ;
ECHA InfoCard	100.034.568
KEGG	C14289 ;
PubChem CID	26541;
UNII	0A7W45JCS9 ;
CompTox Dashboard (EPA)	DTXSID6022428 ;
	InChI 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 Key: YSSSPARMOAYJTE-UHFFFAOYSA-N ; InChI=1/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 Key: YSSSPARMOAYJTE-UHFFFAOYAB;
	SMILES O1c3c(OCCOCCOc2ccccc2OCCOCC1)cccc3;
Properties
Chemical formula	C20H24O6
Molar mass	360.406 g·mol−1
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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	Infobox references

Dibenzo-18-crown-6 is a benzannulated crown ether. It is related to the non-benzannulated 18-crown-6. This compound may be synthesized from catechol and bis(chloroethyl) ether:.[1] This crown ether, like other crown ethers, has strong complexing abilities and has high affinity for alkali metal cations.

References

Charles J. Pedersen (1988). "Macrocyclic Polyethers: Dibenzo-18-Crown-6 Polyether and Dicyclohexyl-18-Crown-6 Polyether". Organic Syntheses.; Collective Volume, 6, p. 395

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[1] Charles J. Pedersen (1988). "Macrocyclic Polyethers: Dibenzo-18-Crown-6 Polyether and Dicyclohexyl-18-Crown-6 Polyether". Organic Syntheses.; Collective Volume, 6, p. 395