15486-62-1Relevant articles and documents
Synthesis, growth, spectral, thermal, mechanical and optical properties of 4-chloro-4′dimethylamino-benzylidene aniline crystal: A third order nonlinear optical material
Leela,Ramamurthi,Bhagavannarayana
, p. 78 - 83 (2009)
An organic nonlinear optical material, 4-chloro-4′dimethylamino-benzylidene aniline (CDMABA), was synthesized by the condensation of the p-chloroaniline and p-dimethylaminobenzaldehyde. Solubility of CDMABA was determined in acetone at different temperatu
An expeditious one-pot synthesis of substituted phenylazetidin-2-ones in the presence of zeolite
Pagadala, Ramakanth,Meshram, Jyotsna S.,Chopde, Himani N.,Jetti, Venkateshwarlu,Udayini
experimental part, p. 1067 - 1072 (2011/10/31)
In this study, one-pot rapid and efficient series of phenylazetidin-2-ones were synthesized from N,N-dimethylaminobenzaldehyde, different substituted aromatic amines and phenylacetyl chloride in the presence of zeolite catalyst under microwave irradiation. We also reported schiff bases (1a-j) by classical and conventional microwave technique. The titled compounds are evaluated for their antimicrobial properties. The activities are due to Ci=O, Ci-N, linkages in 2-azetidinones. All the compounds have shown comparable antibacterial activities.
Electrochemical Synthesis of Heterocyclic Compounds. 17. Anodic Oxidation of Hydrazones in the Presence of Heteroaromatic and Schiff Bases
Gunic, Esmir,Tabakovic, Ibro
, p. 5081 - 5087 (2007/10/02)
Anodic oxidation of a series of hydrazones in the presence of heteroaromatic and Schiff bases were performed in acetonitrile-tetraethylammonium perchlorate electrolyte solution at platinum using controlled potentials.As a result of four-electron oxidation several s-triazolopyridinium perchlorates (1-9), s-triazoloquinolinium perchlorate (10), s-triazoloisoquinolinium perchlorate (11), and s-triazolobenzoquinolinium perchlorate (12) were obtained in yields ranging from 30percent to 90percent.As a result of two-electron oxidation of -p-nitrophenylhydrazine (A) in the presence of imidazole and 1,2,4-triazole the azo derivatives 13 and 14 were obtained with high yields.As a result of two-electron oxidation of hydrazone A in the presence of Schiff bases the new Schiff bases 15-20 were obtained in high yields.On the bases of the electroanalytical and preparative results it is concluded that the electrochemical oxidation of hydrazone A in the presence of heteroaromatic and Schiff bases occurs through the formation of cation B, which is attacked by base as a nucleophile.This excludes the possibility of annelation of the heteroaromatics through nitrilimine as an intermediate.
