54638-91-4

Basic information

• Product Name: Phenol, 2-[(3-phenyl-2-propenylidene)amino]-
• CAS NO: 54638-91-4
• Molecular Formula: C15H13NO
• Molecular Weight: 223.274
• Mol File: 54638-91-4.mol
• Article Data: 10

Chemical Properties

• CAS DataBase Reference: Phenol, 2-[(3-phenyl-2-propenylidene)amino]-(CAS DataBase Reference)
• NIST Chemistry Reference: Phenol, 2-[(3-phenyl-2-propenylidene)amino]-(54638-91-4)
• EPA Substance Registry System: Phenol, 2-[(3-phenyl-2-propenylidene)amino]-(54638-91-4)

Safety Data

• Hazardous Substances Data: 54638-91-4(Hazardous Substances Data)

Upstream product

• 104-55-2 3-phenyl-propenal 
• 95-55-6 2-amino-phenol 
• 141-97-9 ethyl acetoacetate 
• 694472-13-4 trans-N-(3-Phenyl-2-propenylidene)-o-aminophenol 

Downstream Products

• 888-92-6 2-styrylbenzo[d]oxazole 

Relevant articles and documents

Cinnamylaldehyde derivative fluorescent probe compound as well as preparation method and application thereof

The invention discloses a cinnamylaldehyde derivative fluorescent probe compound, a preparation method and application thereof. The cinnamylaldehyde derivative fluorescent probe compound has a structural formula shown in the specification, the cinnamylald

New hockey stick shaped amino allylidene (?N?CH?CH?CH) based compounds: Effect of linkage group on mesomorphic properties

Two nonlinear hockey stick shaped homologous series based on three linking groups have been synthesized and characterized by elemental analyses and spectroscopic techniques. The mesomorphic properties of these compounds were observed by polarizing optical microscopy (POM) and differential scanning calorimetry (DSC). In this present investigation, we have synthesized two homologous series viz. 2-((3-phenyl allylidene) amino) phenyl 4-((4-n-alkoxy benzylidene) amino) benzoate (series-1) and 4-((2-((3-phenyl allylidene) amino) phenoxy) carbonyl) phenyl-4-n-alkoxy benzoate (series-2). Both the series are differing with respect to first linking group. In series-1, comp.C4-C18 shows nematic as well as smectic phase while in series-2, comp.C10-C16 shows smectic and nematic phase while comp.C4-C18 shows only nematic phase.

Mixed ligand complexes with 4-aminoantipyrine derivatives to combat natural antioxidant system: Synthesis, characterization and biological studies

Novel 4-aminoantipyrine based mixed ligand metal complexes with the Schiff bases of L1 (L1-4-aminoantipyrine with furfuraldehyde and L2/L3/L4/L5 are and L2-2-aminophenol with salicylaldehyde, L3-2-aminophenol with cinnamaldehyde, L4-2-aminobenzothiazole with salicylaldehyde, L5-2-aminobenzothiazole with cinnamaldehyde) were synthesized. The structures of the mixed ligand complexes were established by analytical and spectral techniques. They were screened for in vitro antimicrobial activity against of bacteria and fungi by disc diffusion method. The interaction of metal complexes with calf thymus-DNA (CT-DNA) was investigated by UV-visible, cyclic voltammetry, viscosity and thermal denaturation studies. DNA interaction studies suggest that metal complex binds to calf thymus-DNA through intercalation mode. Superoxide dismutase activity of these complexes has also been studied. The free ligands and their metal complexes have been tested for in vitro antioxidant activity by the reduction of 1,1-diphenyl-2-picryl hydrazyl (DPPH). The antioxidant activities of the complexes were studied and compared with the activity of ascorbic acid. Copper(II) complex showed superior antioxidant activity than other complexes.