92968-42-8

Basic information

• Product Name: 3H-Pyrazol-3-one, 4-[(2-furanylmethylene)amino]-1,2-dihydro-1,5-dimethyl-2-phenyl-
• CAS NO: 92968-42-8
• Molecular Formula: C16H15N3O2
• Molecular Weight: 281.314
• Mol File: 92968-42-8.mol
• Article Data: 22

Chemical Properties

• CAS DataBase Reference: 3H-Pyrazol-3-one, 4-[(2-furanylmethylene)amino]-1,2-dihydro-1,5-dimethyl-2-phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: 3H-Pyrazol-3-one, 4-[(2-furanylmethylene)amino]-1,2-dihydro-1,5-dimethyl-2-phenyl-(92968-42-8)
• EPA Substance Registry System: 3H-Pyrazol-3-one, 4-[(2-furanylmethylene)amino]-1,2-dihydro-1,5-dimethyl-2-phenyl-(92968-42-8)

Safety Data

• Hazardous Substances Data: 92968-42-8(Hazardous Substances Data)

Upstream product

• 98-01-1 furfural 
• 83-07-8 4-amino-2,3-dimethyl-1-phenylpyrazolin-5-one 

Downstream Products

• 198631-70-8 [Pr(4-N-(2'-furfurylidene)aminoantipyrine)3(ClO₄)2] perchlorate 
• 128317-58-8 4-(2-(furan-2-yl)-4-oxothiazolidin-3-yl)-1,2-dihydro-2,3-dimethyl-1-phenylpyrazol-5-one 
• 198631-76-4 [Sm(4-N-(2'-furfurylidene)aminoantipyrine)3(ClO₄)2] perchlorate 
• 198631-93-5 [Er(4-N-(2'-furfurylidene)aminoantipyrine)3(ClO₄)2] perchlorate 
• 198631-82-2 [Gd(4-N-(2'-furfurylidene)aminoantipyrine)3(ClO₄)2] perchlorate 
• 198631-90-2 [Ho(4-N-(2'-furfurylidene)aminoantipyrine)3(ClO₄)2] perchlorate 
• 198631-86-6 [Dy(4-N-(2'-furfurylidene)aminoantipyrine)3(ClO₄)2] perchlorate 
• 198631-73-1 [Nd(4-N-(2'-furfurylidene)aminoantipyrine)3(ClO₄)2] perchlorate 
• 198631-79-7 [Eu(4-N-(2'-furfurylidene)aminoantipyrine)3(ClO₄)2] perchlorate 
• 198631-67-3 [La(4-N-(2'-furfurylidene)aminoantipyrine)3(ClO₄)2] perchlorate 
• 232618-96-1 Cu(C₁₆H₁₅O₂N₃)Cl₂*H₂O 

Relevant articles and documents

Synthesis, spectral-characterization, biological and DFT studies of mixed ligand metal(II) complexes of 1,10-phenanthroline bearing 2-aminothiazole moiety

The Schiff base ligand L is developed from furan-2-carboxaldehyde, 4-aminoantipyrine together with 2-aminothiazole. The mixed ligand complexes are developed from the condensation of above Schiff base ligand L, 1,10-phenanthroline as well as metal(II) acet

Characterization of antimicrobial, antioxidant, and leishmanicidal activities of Schiff base derivatives of 4-aminoantipyrine

Our main interest is the characterization of compounds to support the development of alternatives to currently marketed drugs that are losing effectiveness due to the development of resistance. Schiff bases are promising biologically interesting compounds

Synthesis, characterization and antibacterial studies of oxovanadium complexes of tetradentate Schiff base derived from 4-aminoantipyrine, o-phenylene diamine and vanillin/furfural

Two new vanadyl complexes were synthesized from tetradentate Schiff bases having four nitrogens act as donor atoms using 4-aminoantipyrine, o-phenylenediamine and vanillin/furfural. These complexes were characterized by elemental analysis, FTIR, UV-visibl