134592-05-5

Basic information

• Product Name: 9-[(E)-2-(4-nitrophenyl)ethenyl]acridine
• Synonyms: 9-[(E)-2-(4-nitrophenyl)ethenyl]acridine
• CAS NO: 134592-05-5
• Molecular Weight: 326.354
• Mol File: 134592-05-5.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: 9-[(E)-2-(4-nitrophenyl)ethenyl]acridine(CAS DataBase Reference)
• NIST Chemistry Reference: 9-[(E)-2-(4-nitrophenyl)ethenyl]acridine(134592-05-5)
• EPA Substance Registry System: 9-[(E)-2-(4-nitrophenyl)ethenyl]acridine(134592-05-5)

Safety Data

• Hazardous Substances Data: 134592-05-5(Hazardous Substances Data)

Upstream product

• 611-64-3 9-methyl-acridine 
• 555-16-8 4-nitrobenzaldehdye 
• 1556-34-9 9-(bromomethyl)acridine 
• 885-23-4 9-acridincarboxaldehyde 
• 22188-24-5 diethyl (acridin-9-ylmethyl)phosphonate 

Downstream Products

• 134591-99-4 (E)-9-(4-aminostyryl)acridine 

Relevant articles and documents

Synthesis, spectral characterization, DNA binding ability and anti-cancer screening of new acridine-based derivatives

In this study, a series of newly synthesized acridine derivatives, compounds 4, 6a, and 6b, are described and their biological activity on HL-60 cell lines is assessed using a number of different techniques. Binding studies were also performed between the

Hammett type correlations for intramolecular charge transfer (ICT) dipole moments of 4'-substituted 9-styrylacridines in the ground state and in the excited state

9-Styrylacridine(1a) and a series of 4'-substituted 9-styrylacridines (1b-f) (substituent: Me, OMe, NMe2, Cl, NO2) have been prepared to study their spectroscopic properties in several solvents of different dipolarity. They show stro

Thermal Isomerization of Photochemically Synthesized (Z)-9-Styrylacridines. An Unusuallly High Enthalpy of Z -> E Conversion for Stilbene-like Compounds

Eight stable (Z)-9-styrylacridines, have been photochemically synthesized and their enthalpies of thermal isomerization (ΔHZ->E) determined by means of thermal analysis.The enthalpy values were found to be influenced by both electronic and steric effects.The title compounds were used as models in order to gain insight into the energetic implications involved in the Z->E isomerization process and its applicability to photochemical energy conversion by irradiation in the visible wavelength region.