56243-20-0

Upstream product

• 14371-10-9 (E)-3-phenylpropenal 
• 95-54-5 1,2-diamino-benzene 
• 104-55-2 3-phenyl-propenal 

Downstream Products

• 102164-27-2 N-(3-phenyl-propyl)-N,N'-o-phenylene-bis-acetamide 
• 101587-44-4 acetic acid-[2-(3-phenyl-propylamino)-anilide] 
• 102025-08-1 acetic acid-(2-trans-cinnamylidenamino-anilide) 
• 856997-25-6 N-(3-phenyl-propyl)-o-phenylenediamine 
• 58758-09-1 (E)-2-styryl-1H-benzo[d]imidazole 

Relevant academic research and scientific papers

Dehydrogenations using benzofuroxan as oxidant

2-Arylsubstituted benzimidazoles, quinoxalines, in 3,5-position substituted 2,6-dimethylpyridines, and 1,4-bis(alkylamino)-9,10-anthracenediones are easily prepared under mild conditions by means of benzofuroxan as oxidant. Thus, the preparation of 2-arylbenzimidazoles succeeds in acetonitrile at 50°C in yields of 65 to 78%.

Synthesis, characterization, structure, ab initio and DFT calculations of 2-amino-N-(3-phenylprop-2-enylidene)aniline

New Schiff base compound 2-amino-N-(3-phenylprop-2-enylidene)aniline, 1, was prepared by condensation of cinnamaldehyde with o-phenylenediamine and characterized by elemental analyses, UV-Vis and FT-IR spectroscopy. The crystal structure of 1 was determin