61098-06-4Relevant academic research and scientific papers
Synthesis, characterization, and biological evaluation of Schiff base-platinum(II) complexes
Shiju,Arish,Bhuvanesh,Kumaresan
, p. 213 - 222 (2015)
The platinum complexes of Schiff base ligands derived from 4-aminoantipyrine and a few substituted aldehydes were synthesized and characterized by elemental analysis, mass, 1H NMR, IR, electronic spectra, molar conductance, and powder XRD. The
Synthesis of 4-amino-1,5-dimethyl-2-phenylpyrazolone derivatives and their antioxidant activity
Khan, Khalid Mohammed,Khan, Akbar,Taha, Muhammad,Salar, Uzma,Hameed, Abdul,Ismail, Nor Hadiani,Jamil, Waqas,Saad, Syed Muhammad,Perveen, Shahnaz,Kashif, Syed Muhammad
, p. 802 - 810 (2016/01/12)
Schiff bases of 4-amino-1,5-dimethyl-2-phenylpyrazolone (2-18) were synthesized by treating with different benzaldehyde derivatives and tested for in vitro antioxidant activity. Synthesized Schiff base derivatives (2-18) were characterized by various spec
Synthesis and antimicrobial activity of some 4-thiazolidinones
Trivedi, G. S.,Desai, N. C.
, p. 366 - 369 (2007/10/02)
4-Thiazolidinones have been prepared by the reaction of mercaptoacetic acids with anils or with aldehydes and amines.The structures of some of the 4-thiazolidinones (III-V) have been established on the basis of their elemental analyses and spectral data.T
Synthesis and pharmacological screening of a new series of 3-(4-antipyryl)-2-arylthiazolidin-4-ones
Al-Khamees, Hamad A.,Bayomi, Said M.,Kandil, Hesham A.,El-Tahir, Kamal E. H.
, p. 103 - 106 (2007/10/02)
A series of 3-(4-antipyryl)-2-arylthiazolidin-4-one derivatives were synthesized and pharmacologically evaluated for antinociceptive, spasmolytic and cardiovascular activities.The presence of a methoxy-naphthyl or a substituted phenyl group in 2-position
REACTION OF SCHIFF BASES OBTAINED FROM 4-AMINOANTIPYRINE AND 4-AMINO-1,2,4-TRIAZOLE WITH KETONES
Letunov, V. I.
, p. 145 - 149 (2007/10/02)
With acetophenone and p-nitroacetophenone in alcohol and benzene media in the presence of acid N-arylidene-4-aminoantipyrines form α,β-unsaturated ketones, and with antipyrine the form aryldiantipyrylmethanes.With the same ketones N-arylidene-4-amino-1,2,4-triazoles form the products from addition at the azomethine bond.In both cases reaction with benzylideneacetone was not detected.
