85573-09-7

Basic information

• Product Name: N-(4-hydroxybenzylidene)benzene-1,2-diamine
• Synonyms: N-(4-hydroxybenzylidene)benzene-1,2-diamine
• CAS NO: 85573-09-7
• Molecular Weight: 212.251
• Mol File: 85573-09-7.mol
• Article Data: 8

Chemical Properties

• CAS DataBase Reference: N-(4-hydroxybenzylidene)benzene-1,2-diamine(CAS DataBase Reference)
• NIST Chemistry Reference: N-(4-hydroxybenzylidene)benzene-1,2-diamine(85573-09-7)
• EPA Substance Registry System: N-(4-hydroxybenzylidene)benzene-1,2-diamine(85573-09-7)

Safety Data

• Hazardous Substances Data: 85573-09-7(Hazardous Substances Data)

Upstream product

• 123-08-0 4-hydroxy-benzaldehyde 
• 95-54-5 1,2-diamino-benzene 

Downstream Products

• 6504-13-8 4-(1H-benzimidazol-2-yl)phenol 

Relevant articles and documents

Synthesis and evaluation of 2-aryl-1H-benzo[d]imidazole derivatives as potential microtubule targeting agents

Microtubule targeting agents (MTAs) are the potential drug candidates for anticancer drug discovery. Disrupting the microtubule formation or inhibiting the de-polymerization process by a synthetic molecule can lead to an excellent anticancer drug candidat

Ni nanoparticles: Mild and efficient catalyst for the chemoselective synthesis of 2-arylbenzimidazoles, 2-arylbenzothiazoles, and azomethines

(Chemical Equation Presented) A new and efficient method has been developed for the synthesis of biologically significant 2-arylbenzimidazoles, 2-arylbenzothiazoles, and azomethines using recyclable and inexpensive polyvinyl pyrrolidone (PVP)-stabilized Ni nanoparticles in ethylene glycol at room temperature in excellent yields. Copyright Taylor & Francis Group, LLC.

Synthesis and antibacterial activities of some schiff bases

Schiff bases p-hydroxybenzylidene-2-carboxyaniline, p-nitrobenzylidene-2- carboxyaniline, p-(N, N-dimethyl)aminobenzylidene-2-carboxyaniline, N-(4-hydroxybezylidene)-benzene-1,2-diamine, N-(4-nitrobezylidene)benzene-1,2- diamine,N-(4-(N, N-dimethylaminobezylidene)benzene-1,2-diamine, N-(4-(N,Ndimethylamino) benzylidene)naphthalen-1-amine,N-(4-nitrobenzylidene) naphthalen-1-amine,N-(4-chlorobenzylidene)naphthalen-1-amine,sodium-4-(4-(N, N-dimethyl amino)benzylideneamino)naphthalene-1-sulfonate,sodium -4-(4-nitrobenzylideneamino) naphthalene-1-sulfonate and sodium-4-(4- chlorobenzylideneamino) naphthalene-1-sulfonate obtained by condensation of aniline and naphthylamine derivatives with some aromatic aldehydes were characterized by physical and spectral methods. The biological activity of these products were as antibacterial agents against three species of human pathogenic bacteria such as Escherichia coli, Staphylococcus aureus and Klebsiella sp. Nearly 50% of these compounds showed reasonable activity against the bacterial species investigated and we found that the antibacterial activity is dependent on the molecular structure of the compounds.