83-17-0

Basic information

• Product Name: 4-BENZYLIDENEAMINOANTIPYRINE
• Synonyms: 4-BENZYLIDENEAMINOANTIPYRINE
• CAS NO: 83-17-0
• Molecular Formula: C₁₈H₁₇N₃O
• Molecular Weight: 291.34708
• Mol File: 83-17-0.mol
• Article Data: 25

Chemical Properties

• Boiling Point: 421.1°C at 760 mmHg
• Flash Point: 208.5°C
• Appearance: /
• Density: 1.12g/cm³
• Vapor Pressure: 2.68E-07mmHg at 25°C
• Refractive Index: 1.606
• CAS DataBase Reference: 4-BENZYLIDENEAMINOANTIPYRINE(CAS DataBase Reference)
• NIST Chemistry Reference: 4-BENZYLIDENEAMINOANTIPYRINE(83-17-0)
• EPA Substance Registry System: 4-BENZYLIDENEAMINOANTIPYRINE(83-17-0)

Safety Data

• Hazardous Substances Data: 83-17-0(Hazardous Substances Data)

Usage

InChI:InChI=1/C18H17N3O/c1-14-17(19-13-15-9-5-3-6-10-15)18(22)21(20(14)2)16-11-7-4-8-12-16/h3-13H,1-2H3/b19-13+

Upstream product

• 83-07-8 4-amino-2,3-dimethyl-1-phenylpyrazolin-5-one 
• 100-52-7 benzaldehyde 
• 60-80-0 antipyrine 
• 885-11-0 1,5-dimethyl-4-nitroso-2-phenyl-1,2-dihydro-pyrazol-3-one 

Downstream Products

• 14384-36-2 benzylidene-3-aminocarbazole 
• 1861-84-3 1,5,1',5'-tetramethyl-2,2'-diphenyl-1,2,1',2'-tetrahydro-4,4'-phenylmethanediyl-bis-pyrazol-3-one 
• 112591-95-4 UO₂(C₁₈H₁₇N₃O)2(NO₃)2 

Relevant articles and documents

Synthesis, molecular structure and antioxidant activity of (E)-4-[Benzylideneamino]-1,5-dimethyl-2-phenyl-1H-pyrazol-3(2H)-one, a Schiff base ligand of 4-aminoantipyrine

In this study, the title compound, C18H17N 3O (M r = 291.35), was synthesized by the condensation reaction of 4-amino-1,5-dimethyl-2-phenylpyrazole-3-one and benzaldehyde. Single-crystal X-ray diffraction data r

Synthesis, Spectroscopy, and Anticancer Activity of Two New Nanoscale Au(III) N4 Schiff Base Complexes

Mononuclear Au(III) Schiff base complexes are synthesized by the reaction of 4-aminoantipyrine with hydrazine. The chemical structures of new Schiff bases and their Au(III) complexes are elucidated from their conductance, XRD, and spectroscopic (IR, UV-Vi

Preparation of a simple biocompatible magnetite@citric acid: An efficient reusable solid acid catalyst for the rapid synthesis of antipyrine Schiff’s bases and study of their radical scavenging potential

Citric acid immobilized magnetic nanoparticles (MNPs@CA) have been synthesized and used for the preparation of bio-important antipyrine (1,5-dimethyl-2-phenyl-1,2-dihydro-3H-pyrazol-3-one) derived Schiff’s bases (3a–k) in lesser reaction time with very hi

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