58337-98-7

Basic information

• Product Name: 1,2,5-triphenylpentane-1,5-dione
• CAS NO: 58337-98-7
• Molecular Formula: C₂₃H₂₀O₂
• Molecular Weight: 328.4037
• Mol File: 58337-98-7.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 509.4°C at 760 mmHg
• Flash Point: 188.1°C
• Density: 1.127g/cm³
• Vapor Pressure: 1.7E-10mmHg at 25°C
• Refractive Index: 1.599
• CAS DataBase Reference: 1,2,5-triphenylpentane-1,5-dione(CAS DataBase Reference)
• NIST Chemistry Reference: 1,2,5-triphenylpentane-1,5-dione(58337-98-7)
• EPA Substance Registry System: 1,2,5-triphenylpentane-1,5-dione(58337-98-7)

Safety Data

• Hazardous Substances Data: 58337-98-7(Hazardous Substances Data)

Usage

Type of compound

Beta-diketone

Structure

Contains two ketone groups separated by a carbon-carbon bond

Usage

Different sources of media describe the Usage of 58337-98-7 differently. You can refer to the following data:
1. Building block in organic synthesis
2. Ligand in coordination chemistry

Application

Different sources of media describe the Application of 58337-98-7 differently. You can refer to the following data:
1. Preparation of complex organic compounds
2. Reagent in the production of pharmaceuticals and agrochemicals

Potential applications

Different sources of media describe the Potential applications of 58337-98-7 differently. You can refer to the following data:
1. Industrial processes
2. Materials science

Unique properties

Due to its chemical structure and properties

Upstream product

• 451-40-1 phenyl benzyl ketone 
• 936-59-4 3-chloropropiophenone 
• 5724-15-2 N-(2-benzoylethyl)-N,N,N-trimethylammonium iodide 
• 100-42-5 styrene 
• 93-58-3 benzoic acid methyl ester 
• 120-46-7 1,3-diphenylpropanedione 
• 3923-51-1 1,1-diphenylprop-2-en-1-ol 
• 98-86-2 acetophenone 
• 86387-72-6 phenyl(2,5,6-triphenyl-3,4-dihydro-2H-pyran-2-yl)methanone 
• 4452-11-3 1,2-diphenylprop-2-en-1-one 
• 768-03-6 Phenyl vinyl ketone 
• 115963-83-2 2-hydroxy-1,2,5,6-tetraphenyl-hexane-1,6-dione 

Downstream Products

• 37786-68-8 2,3,6-triphenylpyridine 
• 65102-38-7 1,2,3-triphenyl-cyclopentane-1,2-diol 
• 4982-35-8 1,2,3-triphenylcyclopentadiene 

Relevant articles and documents

Metal-free [3 + 2 + 1] annulation of allylic alcohols, ketones, and ammonium acetate: radical-involving synthesis of 2,3-diarylpyridine derivatives

A three-component [3 + 2 + 1] annulation strategy for the synthesis of biologically and pharmaceutically active 2,3-diarylpyridine derivatives by using a series of allylic alcohols, ketones, and ammonium acetate as substrates has been developed. The method proceeds efficiently under metal-free conditions, and the desired heterocycles could be obtained in a site-specific selectivity manner with good functional group tolerance.

Metal-free oxidative radical addition of carbonyl compounds to a,a-Diaryl allylic alcohols: Synthesis of highly functionalized Ketones

A metal-free direct alkylation of simple carbonyl compounds (ketones, esters, and amides) with a,a-diaryl allylic alcohols is described. The protocol provides facile access to highly functionalized dicarbonyl ketones by a radical addition/1,2-aryl migration cascade. The regioselectivity of the reaction was precisely controlled by the nature of the carbonyl compound.