Melting point	49-53 ºC

Symbol(GHS)	Xi
Hazard Codes	R36/37/38
SDS/MSDS	S26;S36

Source	SDS/MSDS Samples
没有数据	没有数据

Synthetic Route

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Name	CAS

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Articles

Peer-Reviewed Papers

Synthesis, characterization and biological studies of Co (II), Ni (II), Cu (II) and Zn (II) complexes with bidentate Schiff bases derived by heterocyclic ketone.Singh K, et al. European Journal of Medicinal Chemistry, 41(1), 147-153 (2006) 2-Acetylpyridine thiosemicarbazones are potent iron chelators and antiproliferative agents: redox activity, iron complexation and characterization of their antitumor activity.Richardson D R, et al. Journal of Medicinal Chemistry, 52(5), 1459-1470 (2009) A europium (III) complex as an efficient singlet oxygen luminescence probe.Song B, et al. Journal of the American Chemical Society, 128(41), 13442-13450 (2006) A near-infrared neutral pH fluorescent probe for monitoring minor pH changes: imaging in living HepG2 and HL-7702 cells.Tang B, et al. Journal of the American Chemical Society, 131(8), 3016-3023 (2009) Evaluation of the cell cytotoxicity and DNA/BSA binding and cleavage activity of some dioxidovanadium(V) complexes containing aroylhydrazones.Subhashree P Dash et al.Journal of inorganic biochemistry, 144, 1-12 (2015-01-13) Reactivity of dinuclear copper(II) complexes towards melanoma cells: Correlation with its stability, tyrosinase mimicking and nuclease activity.Cléia Justino Nunes et al.Journal of inorganic biochemistry, 149, 49-58 (2015-05-30) Comparative photo-release of nitric oxide from isomers of substituted terpyridinenitrosylruthenium(II) complexes: experimental and computational investigations.Joëlle Akl et al.Dalton transactions (Cambridge, England : 2003), 43(33), 12721-12733 (2014-07-12) Synthesis, luminescence, and electrochemical studies of a new series of octanuclear ruthenium(II) complexes of tolylterpyridine appended calixresorcarenes.Selvam Amudhan Senthan et al.Dalton transactions (Cambridge, England : 2003), 44(33), 14813-14822 (2015-07-30) Self-assembled hybrid metal oxide base catalysts prepared by simply mixing with organic modifiers.Masazumi Tamura et al.Nature communications, 6, 8580-8580 (2015-10-06)

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