118965-36-9

Upstream product

• 3489-11-0 6-methylflavanone 
• 4346-94-5 thiosemicarbazide hydrochloride 

Downstream Products

• 1452877-03-0 [Co(6-methyl-2-phenyl-4H-chromen-4-thiosemicarbazone)2Cl₂] 
• 1452877-04-1 [Co(6-methyl-2-phenyl-4H-chromen-4-thiosemicarbazone)2Br₂] 
• 1452877-05-2 [Co(6-methyl-2-phenyl-4H-chromen-4-thiosemicarbazone)2I₂] 
• 1452877-06-3 [Co(6-methyl-2-phenyl-4H-chromen-4-thiosemicarbazone)22(NO₃)2] 
• 1452877-07-4 [Ni(6-methyl-2-phenyl-4H-chromen-4-thiosemicarbazone)2Cl₂] 
• 1452877-08-5 [Ni(6-methyl-2-phenyl-4H-chromen-4-thiosemicarbazone)2Br₂] 
• 1452877-09-6 [Ni(6-methyl-2-phenyl-4H-chromen-4-thiosemicarbazone)2I₂] 
• 1452877-10-9 [Ni(6-methyl-2-phenyl-4H-chromen-4-thiosemicarbazone)22(NO₃)2] 
• 1452877-11-0 [Cu(6-methyl-2-phenyl-4H-chromen-4-thiosemicarbazone)2Cl₂] 
• 1452877-12-1 [Cu(6-methyl-2-phenyl-4H-chromen-4-thiosemicarbazone)2Br₂] 
• 1452877-13-2 [Cu(6-methyl-2-phenyl-4H-chromen-4-thiosemicarbazone)22(NO₃)2] 

Relevant academic research and scientific papers

Spectroscopic and biocidal study of Co(II), Cu(II) and Ni(II) chelates of nitrogen and sulphur containing Schiff base derived from 6-methyl-2-phenyl-4H- chromen-4-one

In the present paper, a series of complex of the type [MLX2] where M = Co(II), Ni(II) and Cu(II), L = 6-methyl-2-phenyl-4H-chromen 4-thisemicarbazone (MPCT) have been synthesized. Their structure were confirmed by means of IR, electronic spectra, elemental analysis and molar conductance, coupled with magnetic susceptibility measurements. All the compounds were assayed for antibacterial activities against one gram positive bacterial strain Bacillus subtilis and one gram negative bacterial strain Eschericpia coli, using disc diffusion technique. It was observed on comparison with reference to antibiotic and fungicides. The complexes were found to be more effective than ligands.