72686-15-8

Usage

Physical appearance

White crystalline powder The compound's visual appearance is that of a white, crystalline solid.

Solubility

Insoluble in water, soluble in organic solvents The compound does not dissolve well in water but can dissolve in certain organic solvents.

Applications

Synthesis of pharmaceuticals and agrochemicals 1H-Inden-1-one, 3-benzoyl-2-phenylis used as a building block or intermediate in the production of various drugs and agricultural chemicals.

Applications

Production of dyes and pigments The compound is also used in the creation of colorants for various industries.

Biological activities

Anti-inflammatory properties 1H-Inden-1-one, 3-benzoyl-2-phenylhas been found to help reduce inflammation in biological systems.

Biological activities

Anti-tumor properties The compound has shown potential in inhibiting or preventing the growth of tumors.

Potential uses

Development of new materials Researchers are exploring the use of 1H-Inden-1-one, 3-benzoyl-2-phenylin creating novel materials with unique properties.

Potential uses

Organic synthesis reagent The compound is being investigated as a reagent in organic synthesis, which could lead to the development of new chemical reactions and processes.

Upstream product

• 72686-14-7 o-Phenylendiacetophenon 
• 13203-60-6 1,2-bis(2-phenylethynyl)benzene 
• 91-13-4 α,α'-dibromo-o-xylene 
• 613-73-0 1,2-phenylenediacetonitrile 
• 41640-86-2 2,2’-(1,2-phenylene)diacetyl chloride 
• 7500-53-0 1,2-Phenylenediacetic acid 
• 67-63-0 isopropyl alcohol 
• 64-17-5 ethanol 
• 67-56-1 methanol 

Relevant academic research and scientific papers

I2O5-Mediated 1,5-Cyclization of Aryldiynes with H2O: A Way to Access 3-Acyl-1-indenone Derivatives

A facile I2O5-mediated 1,5-cyclization of aryldiynes with H2O has been successfully developed, leading to a broad range of substituted 3-acyl-1-indenones in moderate to excellent yields. The protocol has advantages of a me

A synthetic method for preparing compound ketone group (by machine translation)

The invention provides a method for preparing compound ketone group of the preparation method. The synthetic method is formula (I) indicated by the diyne compound as a raw material, with the participation of water, in order to five oxidation b iodine is t

A 3 - [...] ketone compounds

The invention provides a 3 - [...] ketone compound. The synthetic method is formula (I) indicated by the diyne compound as a raw material, the metal copper in presence, to Selectcfluor as the oxidizing agent, acetonitrile as solvent, in the 25 °C reaction

Rhodium(III)-catalyzed annulation of azomethine ylides with alkynes via C-H activation

The rhodium(III)-catalyzed coupling of azomethine ylides with alkynes via C-H activation has been developed for the synthesis of indenamines in moderate to high yields. The coupled products can be further oxidized to indenones and derivatives.

Synthesis of benzofulvenes by palladium-catalyzed cyclization of 1,2-dialkynylbenzenes

A palladium-catalyzed cyclization of enediynes for the synthesis of benzofulvenes 2 in yields of 59-76% was accomplished by treatment of dialkynylbenzenes 1 with 5 mol% of PdX2 and 3 equiv. of CuX 2 in acetonitrile at 60 °C for 2 h.

A NEW PHOTO/THERMOCHROMIC SOLID COMPOUND OF THE INDENONE OXIDE FAMILY

A new strong photochromic solid compound, a 3-ketone of the 2,3-diphenylindenone oxide, has been prepared for first time.The new compound exhibits very strong photochromic and thermochromic phenomena.