65565-59-5

Basic information

• Product Name: Methanone, phenyl(4-propoxyphenyl)-
• CAS NO: 65565-59-5
• Molecular Formula: C16H16O2
• Molecular Weight: 240.302
• Mol File: 65565-59-5.mol

Chemical Properties

• CAS DataBase Reference: Methanone, phenyl(4-propoxyphenyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Methanone, phenyl(4-propoxyphenyl)-(65565-59-5)
• EPA Substance Registry System: Methanone, phenyl(4-propoxyphenyl)-(65565-59-5)

Safety Data

• Hazardous Substances Data: 65565-59-5(Hazardous Substances Data)

Upstream product

• 622-85-5 propoxybenzene 
• 98-88-4 benzoyl chloride 
• 71-23-8 propan-1-ol 
• 345-83-5 4-fluorobenzophenone 
• 106-94-5 propyl bromide 
• 1137-42-4 4-Hydroxybenzophenone 

Relevant articles and documents

High-efficiency long-service life organic room-temperature phosphorescence material and preparation method thereof

The invention provides an alkoxy, benzyloxy or bromine substituted xanthone derivative and a preparation method thereof. The xanthone derivative is simple in preparation method, has a phosphorescencepeak on a long wavelength peak and is long in phosphorescence service life and high in light emission efficiency. The preparation method of the xanthone derivative comprises the following preparationsteps: 1, putting phenol, potassium carbonate, DMF (Dimethyl Formamide) and methylbenzene into a reaction container, backflowing for 3-5 hours in a nitrogen environment, and carrying out dehydration treatment till the system has no water generation; removing the methylbenzene, recovering to the room temperature, adding 4-bromine-2-fluorobenzonitrile, backflowing for 3-5 hours in the nitrogen environment, after the reaction is completed, diluting the solution with 100mL of methylbenzene, filtering, washing with water, drying so as to obtain a crude product of a crystal, and purifying with a spectrum column so as to obtain an intermediate as shown in the specification; 2, mixing the intermediate obtained in the step 1 with water and sulfuric acid, heating to 150-200 DEG C in the nitrogen environment, stirring, and backflowing for 10-15 hours; after the reaction is completed, cooling to the room temperature, diluting with water, extracting by using trichloromethane and a saturated sodiumchloride solution, combining organic phases, drying, filtering, carrying out vacuum distillation so as to remove the solvent and obtain a crude product of a crystal, and purifying with a spectrum column, so as to obtain an intermediate as shown in the specification.

Triton B-mediated efficient and convenient alkoxylation of activated aryl and heteroaryl halides

A simple and convenient one-pot synthesis of aryl alkyl ethers by the alkoxylation of aryl halides with alcohol in the presence of Triton B as a base is described. The procedure is applicable for a variety of aryl and heteroaryl halides, and yields are very good. The use of a nonmetallic base and solvent-free conditions are important features of the reaction. Copyright Taylor & Francis Group, LLC.