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P107838-25g1,10-Phenanthroline-5,6-dione (phendio) forms Cu(II) and Ag(I) phendio complexes, which show potent anti-fungal and anti-cancer activity.The modification of glassy carbon (GC) electrodes with phendio complexes of transition metals leads to the
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P107838-5g1,10-Phenanthroline-5,6-dione (phendio) forms Cu(II) and Ag(I) phendio complexes, which show potent anti-fungal and anti-cancer activity.The modification of glassy carbon (GC) electrodes with phendio complexes of transition metals leads to the
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U162901-1ml1,10-Undecadiene.
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U162901-5ml1,10-Undecadiene.
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D154912-1g1,11-Diaminoundecane.
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D154912-200mg1,11-Diaminoundecane.
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D154912-5g1,11-Diaminoundecane.
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D138351-100gUsed in preparation of thermotropic main-chain polyether and has been studied by variable-temperature solid-state 13C NMR spectroscopy among other uses1,11-Dibromoundecane was used in preparation of:• thermotropic main-chain polyether and has been
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D138351-10gUsed in preparation of thermotropic main-chain polyether and has been studied by variable-temperature solid-state 13C NMR spectroscopy among other uses1,11-Dibromoundecane was used in preparation of:• thermotropic main-chain polyether and has been
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D138351-1gUsed in preparation of thermotropic main-chain polyether and has been studied by variable-temperature solid-state 13C NMR spectroscopy among other uses1,11-Dibromoundecane was used in preparation of:• thermotropic main-chain polyether and has been
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D138351-25gUsed in preparation of thermotropic main-chain polyether and has been studied by variable-temperature solid-state 13C NMR spectroscopy among other uses1,11-Dibromoundecane was used in preparation of:• thermotropic main-chain polyether and has been
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D138351-5gUsed in preparation of thermotropic main-chain polyether and has been studied by variable-temperature solid-state 13C NMR spectroscopy among other uses1,11-Dibromoundecane was used in preparation of:• thermotropic main-chain polyether and has been