4614-01-1

Basic information

• Product Name: 1,1,3-triphenyl-1H-indene
• CAS NO: 4614-01-1
• Molecular Formula: C₂₇H₂₀
• Molecular Weight: 344.4477
• Mol File: 4614-01-1.mol
• Article Data: 12

Chemical Properties

• Boiling Point: 475°C at 760 mmHg
• Flash Point: 239.2°C
• Density: 1.145g/cm³
• Vapor Pressure: 9.84E-09mmHg at 25°C
• Refractive Index: 1.661
• CAS DataBase Reference: 1,1,3-triphenyl-1H-indene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1,3-triphenyl-1H-indene(4614-01-1)
• EPA Substance Registry System: 1,1,3-triphenyl-1H-indene(4614-01-1)

Safety Data

• Hazardous Substances Data: 4614-01-1(Hazardous Substances Data)

Usage

Type of compound

Indene, a bicyclic hydrocarbon with a benzene ring fused to a cyclopentadiene ring

Structure

Three phenyl groups attached to the indene ring

Common uses

a. Organic synthesis
b. Production of organic electronic materials
c. Intermediate in the synthesis of pharmaceuticals and agrochemicals

Unique properties

a. Aromatic properties
b. Valuable building block for creating a variety of chemical products

Potential applications

a. Materials science
b. Pharmaceuticals
c. Agrochemicals

Upstream product

• 67-56-1 methanol 
• 1053-23-2 1,1,2,2-tetraphenylcyclopropane 
• 55010-17-8 3,3-diphenyl-indan-1-one 
• 772-62-3 3,3,3-trifluoro-1-phenylpropyne 
• 71-43-2 benzene 
• 76-84-6 triphenylmethyl alcohol 
• 536-74-3 phenylacetylene 
• 86477-15-8 3-methoxy-1,1,3,3-tetraphenylpropene 
• 7338-94-5 1,3-diphenyl-2-propynone 
• 108-86-1 bromobenzene 
• 95-13-6 1-indene 
• 7446-70-0 aluminium trichloride 
• 1674-18-6 tetraphenylallene 
• 67-66-3 chloroform 

Downstream Products

• 40112-66-1 1,1,3-triphenyl-2-indanone 
• 38274-35-0 1,2,3-triphenylindene 
• 56849-86-6 methyl-(1,2,3-triphenyl-inden-1-yl)-ether 
• 31366-67-3 1,2,3-triphenylindan 
• 77387-99-6 2-Brom-1,1,3-triphenylinden 
• 42523-79-5 1,3,3-Triphenyl-indan-2-ol 
• 861523-65-1 (2-benzoyl-phenyl)-diphenyl-acetic acid 
• 73010-42-1 1,1,3-Triphenylindane 

Relevant articles and documents

Microwave-Assisted Condensation of Benzylic Alcohols and Alkynes Promoted by Zinc Halides: Concise Access to Alkenyl Halides

A simple Lewis acid-mediated route for the synthesis of alkenyl halides are described under microwave-assisted conditions. The reaction proceeds through the condensation between secondary alcohols and terminal acetylenes and regioselective hydrohalogenati

Regiocontrolled hydroarylation of (trifluoromethyl)acetylenes in superacids: Synthesis of CF3-substituted 1,1-diarylethenes

The reactions between aryl(trifluoromethyl)-substituted alkynes and arenes in triflic and fluorosulfonic acids were investigated. These reactions proceeded 100 % regioselectively to give 1,1-diaryl-2-trifluoromethylethenes in high yields. Depending on the

Synthesis of substituted indenes from 3-phenyl-2-propyn-1-ol derivatives

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