42866-38-6

Basic information

• Product Name: 4-{[(1E,2E)-3-phenylprop-2-en-1-ylidene]amino}phenol
• CAS NO: 42866-38-6
• Molecular Formula: C₁₅H₁₃NO
• Molecular Weight: 223.2698
• Mol File: 42866-38-6.mol
• Article Data: 6

Chemical Properties

• Boiling Point: 417.5°C at 760 mmHg
• Flash Point: 270.1°C
• Density: 1.01g/cm³
• Vapor Pressure: 1.46E-07mmHg at 25°C
• Refractive Index: 1.556
• CAS DataBase Reference: 4-{[(1E,2E)-3-phenylprop-2-en-1-ylidene]amino}phenol(CAS DataBase Reference)
• NIST Chemistry Reference: 4-{[(1E,2E)-3-phenylprop-2-en-1-ylidene]amino}phenol(42866-38-6)
• EPA Substance Registry System: 4-{[(1E,2E)-3-phenylprop-2-en-1-ylidene]amino}phenol(42866-38-6)

Safety Data

• Hazardous Substances Data: 42866-38-6(Hazardous Substances Data)

Upstream product

• 123-30-8 4-amino-phenol 
• 104-55-2 3-phenyl-propenal 
• 7664-93-9 sulfuric acid 
• 37056-75-0 cinnamaldehyde-(N-phenyl oxime ) 

Downstream Products

• 111761-85-4 [(E)-3-Phenyl-prop-2-en-(Z)-ylidene]-(4-trimethylsilanyloxy-phenyl)-amine 
• 84423-25-6 1-(4-Hydroxy-phenyl)-4a-methoxy-7-(4-methoxy-3,6-dioxo-cyclohexa-1,4-dienyl)-4-phenyl-1,4,4a,8a-tetrahydro-quinoline-5,8-dione 
• 84423-30-3 1,1'-Bis-(4-hydroxy-phenyl)-4a,4'a-dimethoxy-4,4'-diphenyl-1,4,4a,8a,1',4',4'a,8'a-octahydro-[7,7']biquinolinyl-5,8,5',8'-tetraone 
• 111761-86-5 N-(p-dimethyl-t-butylsiloxybenzylidene)styrylamine. 
• 111761-89-8 trans-1-(p-hydroxyphenyl)-3-phthalimidoyl-4-styrylazetidin-2-one 
• 111761-89-8 cis-1-(p-hydroxyphenyl)-3-phthalimidoyl-4-styrylazetidin-2-one 
• 111761-91-2 cis-1-(p-dimethyl-t-butylsiloxyphenyl)-3-phthalimidoyl-4-styrylazetidin-2-one 
• 111761-91-2 trans-1-(p-dimethyl-t-butylsiloxyphenyl)-3-phthalimidoyl-4-styrylazetidin-2-one 
• 84410-22-0 3-Hydroxy-6-(4-hydroxy-phenyl)-2,9a-dimethoxy-9-phenyl-5a,6,9,9a-tetrahydro-11-oxa-6-aza-benzo[b]fluorene-5,10-dione 

Relevant articles and documents

Synthesis of azomethines derived from cinnamaldehyde and vanillin: in vitro aetylcholinesterase inhibitory, antioxidant and insilico molecular docking studies

In the present study, we report the synthesis of azomethines derived from cinnamaldehyde (C1–C3) and vanillin (V1–V3) using ethanol as a green solvent in the presence of triethyl amine. The synthesized compounds were characterized and investigated for the

Antioxidant activities and transition metal ion chelating studies of some hydroxyl Schiff base derivatives

Several hydroxyl Schiff base (HSB) compounds (1-10) with good radical scavenging activity (RSA) were designed. Compounds 6, 7, and 10 showed better RSAs than the common synthetic antioxidant 2,6-diterbutyl- 4-methylphenol (BHT) in DPPH and ABTS assays. To probe whether these HSB compounds may exert their antioxidant effect through transition metal ion chelation, the copper and ferrous chelating abilities of them were investigated. It was found by fluorescence quenching spectra that the binding constants Ka were in the range of 0.85×103-7.30×104 M-1. Further study was carried out by the complexation of a representative compound 5 with ferrous ion in mass spectrum. A 2:1 5-ferrous complex was readily formed in a methanol-water solution (v:v, 8:2), which confirmed that the chelation happened when the HSB compounds were treated with transition metal ions. The above results indicated that the transition metal ion chelation play an important role in their antioxidant abilities. Springer Science+Business Media, LLC 2011.

Synthesis of New Polycyclic Carbazoloquinones

Some new policyclic carbazoloquinones, substituted 6H-pyridocarbazoles (V) have been synthesized by the interaction of the Diels-Alder adducts (II), obtained from the addition of cinnamyliden-anils (I) to 4,4-dimethoxyquinone in 1:1 molar ratio, wi