24776-45-2

Basic information

• Product Name: Methanone, (4-methoxy-1-naphthalenyl)phenyl-
• CAS NO: 24776-45-2
• Molecular Formula: C18H14O2
• Molecular Weight: 262.308
• Mol File: 24776-45-2.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Methanone, (4-methoxy-1-naphthalenyl)phenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Methanone, (4-methoxy-1-naphthalenyl)phenyl-(24776-45-2)
• EPA Substance Registry System: Methanone, (4-methoxy-1-naphthalenyl)phenyl-(24776-45-2)

Safety Data

• Hazardous Substances Data: 24776-45-2(Hazardous Substances Data)

Upstream product

• 56268-83-8 2-(4-Methoxy-naphthalen-1-yl)-1,2-diphenyl-ethanone 
• 90-15-3 α-naphthol 
• 15971-29-6 4-methoxy-1-naphthaldehyde 
• 98-80-6 phenylboronic acid 
• 171258-08-5 2-(phenylethynyl)acetophenone 
• 149-73-5 trimethyl orthoformate 
• 93-97-0 benzoic acid anhydride 
• 2216-69-5 1-Methoxynaphthalene 
• 10075-62-4 1,4-dimethoxynaphthalene 
• 98-88-4 benzoyl chloride 
• 618-32-6 Benzoyl bromide 

Downstream Products

• 70109-45-4 1-Hydroxy-9-methoxy-4-phenyl-phenanthren-3-carbonsaeure 
• 177738-95-3 1-hydroxy-9-methoxy-3-methoxycarbonyl-4-phenylphenanthrene 
• 238-84-6 benzo[a]fluorene 
• 70109-57-8 (E)-3-Carboxy-4-(4-methoxy-<1>naphthyl)-4-phenyl-but-3-en-saeure 
• 70109-39-6 1-Acetoxy-9-methoxy-4-phenyl-phenanthren-3-carbonsaeure-ethylester 
• 62345-25-9 4-methoxynaphthyldiphenylmethanol 
• 24776-44-1 4-benzoyl-1-naphthol 
• 210179-81-0 (4-ethoxy-[1]naphthyl)-phenyl ketone 

Relevant articles and documents

Facile synthesis of regio-isomeric naphthofurans and benzodifurans

Naphtho[1,2-b]furans 1a-f, naphtho[2,1-b]furans 2a-f, benzo[1,2-b:5,4- b′]difurans 3a-b, benzo[1,2-b:4,5-b′]difurans 4a-b, and benzo[1,2-b:4,3-b′]difurans 5a-b were synthesized by base-catalyzed cyclization reaction of the corresponding o-alkoxybenzoylarene derivatives. The o-alkoxybenzoylarenes were obtained from the etherification reaction of the o-hydroxybenzoylarenes, which were prepared either by the reaction of methoxyarenes with benzoyl chloride in the presence of aluminum chloride or by photo-Fries rearrangement of aryl benzoates. Graphical Abstract.

Synthesis and structural characterization of Pd(II) thiosemicarbazonato complex: Catalytic evaluation in synthesis of diaryl ketones from aryl aldehydes and arylboronic acids

A simple route to synthesize triphenylphosphinopalladium(II) thiosemicarbazonato complex has been described. Elemental analysis, spectral (IR, NMR) and single crystal X-ray diffraction techniques were employed for the complete characterization of the complex. The latter was found to be effective catalyst for carbon–carbon cross-coupling reaction of aryl- and heteroarylboronic acids with aromatic and heteroaromatic aldehydes to form the corresponding diaryl ketones. The influence of reaction parameters such as solvent, base, reaction temperature and catalyst loading was also investigated.

Directing zeolite structures into hierarchically nanoporous architectures

Crystalline mesoporous molecular sieves have long been sought as solid acid catalysts for organic reactions involving large molecules. We synthesized a series of mesoporous molecular sieves that possess crystalline microporous walls with zeolitelike frameworks, extending the application of zeolites to the mesoporous range of 2 to 50 nanometers. Hexagonally ordered or disordered mesopores are generated by surfactant aggregates, whereas multiple cationic moieties in the surfactant head groups direct the crystallization of microporous aluminosilicate frameworks. The wall thicknesses, framework topologies, and mesopore sizes can be controlled with different surfactants. The molecular sieves are highly active as catalysts for various acid-catalyzed reactions of bulky molecular substrates, compared with conventional zeolites and ordered mesoporous amorphous materials.