29955-19-9

Upstream product

• 38411-41-5 (3-nitrophenyl)acetyl chloride 
• 100-66-3 methoxybenzene 
• 1877-73-2 3-nitro-benzeneacetic acid 

Downstream Products

• 860538-05-2 1'-(3-aminophenyl)-2'-(4''-methoxyphenyl)ethan-2'-one 
• 153529-27-2 1-(4-Methoxy-phenyl)-2-(3-nitro-phenyl)-ethanol 
• 116503-78-7 1-(methoxyphenyl)-2-(3-nitrophenyl)-3-(3-methoxyphenyl)-1-propanone 
• 153529-10-3 3-[2-Imidazol-1-yl-2-(4-methoxy-phenyl)-ethyl]-phenylamine 
• 153529-06-7 1-[1-(4-Methoxy-phenyl)-2-(3-nitro-phenyl)-ethyl]-1H-imidazole 
• 114584-02-0 2-(3-nitrophenyl)-3-(4-methoxyphenyl)-6-methoxyindene 
• 62043-92-9 4'-methoxy-α'-oxo-bibenzyl-3-carbonitrile 
• 856352-59-5 4'-methoxy-α'-oxo-bibenzyl-3-carboxylic acid 

Relevant academic research and scientific papers

Synthesis of Benzo[ b]furans by Intramolecular C-O Bond Formation Using Iron and Copper Catalysis

One-pot processes for the synthesis of benzo[b]furans from 1-aryl- or 1-alkylketones using nonprecious transition metal catalysts have been developed. Regioselective iron(III)-catalyzed halogenation of the aryl ring, followed by iron- or copper-catalyzed O-arylation allowed the synthesis of various structural analogues, including the benzo[b]furan-derived natural products corsifuran C, moracin F, and caleprunin B.

Design and synthesis of 3-phenyltetrahydronaphthalenic derivatives as new selective MT2 melatoninergic ligands. Part II

Following our studies of the melatoninergic receptors, we have developed new tetrahydronaphthalenic derivatives of melatonin that have been tested as selective melatonin receptors ligands. Regarding the role of the phenyl substituent to obtain selective l

Antifungal agents. 5. Chloro and amino derivatives of 1,2-diaryl-1-(1H-imidazol-1-yl)ethane with potent antifungal activities

Various derivatives of 1,2-diaryl-1-(1H-imidazol-1-yl)ethane have been synthesized and tested against Candida albicans and Candida spp.In vitro essays showed chloro and amino derivatives to be as active as miconazole and bifonazole and more potent than ketoconazole.Structure-activity relationships of the new imidazole antifungal agents are discussed.antifungal agents/estrogen-like imidazoles/1,2-diaryl-1-(1H-imidazol-1-yl)ethane derivatives

Fluorescence properties of 2,3-diarylindenes

The absorbance and fluorescence properties of three 2,3-diarylindenes substituted with donor and acceptor functions were studied and compared with the corresponding donor/acceptor-substituted stilbenes. The parent systems, 2-phenyl-3-(4-methoxyphenyl)-6-m