14290-11-0

Basic information

• Product Name: Propiophenone phenyl hydrazone
• Synonyms: Propiophenone phenyl hydrazone
• CAS NO: 14290-11-0
• Molecular Formula: C₁₅H₁₆N₂
• Molecular Weight: 224.3009
• Mol File: 14290-11-0.mol
• Article Data: 5

Chemical Properties

• Boiling Point: 345°Cat760mmHg
• Flash Point: 162.4°C
• Appearance: /
• Density: 0.99g/cm³
• Vapor Pressure: 6.34E-05mmHg at 25°C
• Refractive Index: 1.555
• CAS DataBase Reference: Propiophenone phenyl hydrazone(CAS DataBase Reference)
• NIST Chemistry Reference: Propiophenone phenyl hydrazone(14290-11-0)
• EPA Substance Registry System: Propiophenone phenyl hydrazone(14290-11-0)

Safety Data

• Hazardous Substances Data: 14290-11-0(Hazardous Substances Data)

Usage

InChI:InChI=1/C15H16N2/c1-2-15(13-9-5-3-6-10-13)17-16-14-11-7-4-8-12-14/h3-12,16H,2H2,1H3

Upstream product

• 100-63-0 phenylhydrazine 
• 93-55-0 1-phenyl-propan-1-one 

Downstream Products

• 10257-92-8 2-phenyl-3-methyl-1H-indole 
• 131366-31-9 5-Ethyl-2,5-diphenyl-[1,2,4]triazolidin-3-one 
• 81323-22-0 N-Phenyl-N'-(1-hydroxylamino-1-phenyl)propylhydrazine 
• 131366-41-1 (1-Isocyanato-1-phenyl-propyl)-phenyl-diazene 
• 6011-26-3 2'-acetylbenzanilide 
• 39608-24-7 3-hydroperoxy-3-methyl-2-phenyl-3H-indole 
• 7189-06-2 (1,3-diphenyl-1H-pyrazol-4-yl)(phenyl)methanone 
• 78830-49-6 (1,3-diphenyl-1H-pyrazol-4-yl)(p-tolyl)methanone 
• 65837-38-9 6-bromo-3-methyl-2-phenyl-indole 
• 81323-40-2 N-Phenyl-N'-(1-amino-1-phenyl)propylhydrazine 
• 3558-28-9 1,3-dimethyl-2-phenyl-1H-indole 
• 34672-83-8 ethoxy-2,2,6,6-tetramethylpiperidine-1 

Relevant articles and documents

Design, synthesis and biological evaluation of hydrazone derivatives as anti-proliferative agents

A series of triaryl-substituted hydrazones as structural acyclic prototypes were synthesized and screened for anti-proliferative activity against breast (Michigan cancer foundation-7 and MD Anderson metastatic breast-231) and uterine cancer (Ishikawa) cel

TEMPO-mediated Aza-diels-alder reaction: Synthesis of tetrahydropyridazines using ketohydrazones and olefins

A novel, facile, and efficient method for the synthesis of tetrahydropyridazines by a one-pot tandem reaction of easily accessible ketohydrazones and olefins in the presence of 2,2,6,6-tetramethylpiperidine-1-oxyl (TEMPO) has been successfully developed. The reaction involves the initial generation of azoalkenes from direct oxidative dehydrogenation of ketohydrazones using TEMPO as the commercially available oxidant, followed by a subsequent aza-Diels-Alder reaction with olefins.

Addition of Dimethyl Acetylenedicarboxylate to 1,2,3-Trisubstituted Indoles having no Hydrogen on the Carbon Atom attached to C-2.

Addition of dimethyl acetylenedicarboxylate to seven 1,2,3-trisubstituted indoles having no hydrogen on the carbon atom attached to C-2, has yielded fourteen adducts which are mainly fused γ-lactones, but which include a new phenanthridine-dione, a novel spiro-dihydroindole, and a carbazole formed by the loss of methane.All structures were elucidated by spectroscopy.