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Lithium ionophore

Crown-4 (lithium ionophore V, 1,4,7,10-tetraoxacyclododecane) [294-93-9] M 176.2, m 17°. The distilled crude product had to be crystd from pentane at -20° to remove acyclic material. It is then dried over P2O5. [Acta Chem Scand 27 3395 1973.]... [Pg.414]

Dibenzyl-14-crown-4 (lithium ionophore VI 6,6-dibenzyl-l,4,8,ll-tetra-oxa-cyclo-tetradecane) [106868-21-7] M 384.5, m 102-103°. Dissolve in CHCI3, wash with saturated aqueous NaCl, dry with MgSOa, evaporate and purify by chromatography on silica gel and gradient elution with C6Hg-MeOH followed by preparative reverse phase HPLC on an octadecyl silanised silica (ODS) column and eluting with MeOH. It can be crystd from MeOH (v Br 120 cm , C-O-C). [7 Chem Soc Perkin Trans 1 1945 1986.]... [Pg.417]

A -Diheptyl-A, A -5,5-tetramethyl-3,7-dioxanonanediamide [lithium ionophore I (ETH 149)] [58821-96-8J M 442.7. Purified by chromatography on Kieselgel using CHCI3 as eluent (IR v 1640cm ). [Helv Chim Acta 60 2326 1977.]... [Pg.419]

Dibenzyl-14-crown-4 (lithium ionophore VI 6,6-dibenzyl-l,4,8,ll-tetra-oxa-cyclo-... [Pg.417]

See other pages where Lithium ionophore is mentioned: [Pg.383]    [Pg.398]    [Pg.398]    [Pg.398]    [Pg.382]    [Pg.383]    [Pg.398]    [Pg.398]    [Pg.398]    [Pg.346]    [Pg.474]    [Pg.414]    [Pg.520]    [Pg.522]    [Pg.408]    [Pg.601]    [Pg.633]    [Pg.636]    [Pg.636]    [Pg.1270]    [Pg.283]   
See also in sourсe #XX -- [ Pg.379 , Pg.382 , Pg.383 ]

See also in sourсe #XX -- [ Pg.379 , Pg.382 , Pg.383 ]

See also in sourсe #XX -- [ Pg.10 , Pg.14 , Pg.601 ]



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14-Crown-4 ionophores, lithium selective

6,6-Dibenzyl-14-crown lithium ionophore

Ionophor

Ionophore

Ionophores

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