2-Chloro-5-nitrobenzaldehyde thiosemicarbazone
Acta Crystallographica Section E, 2010 The title Schiff base compound, C8H7ClN4O2S, was prepared by the reaction of equimolar quantities of 2-chloro-5-nitrobenzaldehyde with thiosemicarbazide in methanol.
Yu-Mei Hao
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4-Hydroxy-3-methoxybenzaldehyde thiosemicarbazone
Acta Crystallographica Section E, 2013 In the title compound, C9H11N3S, there is an intramolecular O—H...O hydrogen bond involving the OH group and the adjacent methoxy O atom. The molecule is essentially planar, with the maximum deviation from the mean plane of the non-H atoms being 0 ...
Inke Jess +3 more
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Synthesis, structural and spectral studies of 5-methyl 2-furaldehyde thiosemicarbazone and its Co, Ni, Cu and Cd complexes [PDF]
, 2001 The reaction of cobalt, nickel, copper and cadmium chlorides and bromides with 5-methylfurfural thiosemicarbazone (M5FTSC) leads to the formation of two series of new complexes: [M(M5FTSC)2X2], [M(M5FTSC)X2]. They have been characterized by spectroscopic
A. Riou +4 more
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4-Methylbenzaldehyde thiosemicarbazone
Acta Crystallographica Section E, 2009 The title compound, C9H11N3S, was prepared by reacting 4-methylbenzaldehyde with thiosemicarbazide. An intramolecular N—H...N hydrogen bond helps to establish the observed molecular conformation.
Jian Zhang +3 more
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4-(3-Nitrophenyl)thiazol-2-ylhydrazone derivatives as antioxidants and selective hMAO-B inhibitors: synthesis, biological activity and computational analysis [PDF]
, 2019 A new series of 4-(3-nitrophenyl)thiazol-2-ylhydrazone derivatives were designed, synthesised, and evaluated to assess their inhibitory effect on the human monoamine oxidase (hMAO) A and B isoforms. Different (un)substituted (hetero)aromatic substituents
Alcaro, Stefano +10 more
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Synthesis and characterization of dioxidomolybdenum(VI) complexes with thiosemicarbazone ligands [PDF]
, 2014 The chemistry of thiosemicarbazone complexes of transition metals has been the subject of attention, primarily because of overgrowing biological properties. These activities have been correlated with their metal-chelating abilities and reductive capacity.
., Shweta
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4-Cyanobenzaldehyde thiosemicarbazone
Acta Crystallographica Section E, 2009 The molecule of the title compound, C9H8N4S, adopts an E configuration about both the C=N and C—NH bonds. In the crystal structure, adjacent molecules are linked by intermolecular N—H...S hydrogen-bonding interactions, forming chains running ...
De-Hong Wu +3 more
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Charge Transfer-oxy Radical Mechanism for Anti-cancer Agents [PDF]
, 1986 The proposal is advanced that anti-cancer drugs generally function by charge transfer resulting in formation of toxic oxy radicals which destroy the neoplasm.
Ames, James R. +5 more
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Functionalizing Thiosemicarbazones for Covalent Conjugation
MoleculesThiosemicarbazones (TSCs) with their modular character (thiosemicarbazides + carbonyl compound) allow broad variation of up to four substituents on the main R1R2C=N(1)–NH–C(S)–N(4)R3R4 core and are thus interesting tools for the formation of conjugates or the functionalization of nanoparticles (NPs). In this work, di-2-pyridyl ketone was introduced for
Johannes Hohnsen +5 more
openaire +3 more sources
Synthesis, Characterisation and Biological Activity Screening Of Schiff Base Ligands Containing Isatin and Their Metal Complexes [PDF]
, 2008 Six new Schiff bases formed from the condensation reaction of S-benzyldithiocarbazate (SBDTC) and S-methyldithiocarbazate (SMDTC) with selected diketones containing isatin derivatives namely isatin, 5-fluroisatin, 5-chloroisatin, 5-bromoisatin and ...
Abdul Manan, Mohd Abdul Fatah
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