18084-97-4

Basic information

• Product Name: chlorotriphenylethylene
• Synonyms: chlorotriphenylethylene;1,1',1''-(1-Chloroethenyl-2-ylidene)trisbenzene;1,1,2-Triphenyl-2-chloroethene;1-Chloro-1,2,2-triphenylethene;1-CHLOROTRIPHENYLETHYLENE
• CAS NO: 18084-97-4
• Molecular Formula: C₂₀H₁₅Cl
• Molecular Weight: 290.7861
• EINECS: 241-992-7
• Mol File: 18084-97-4.mol
• Article Data: 8

Chemical Properties

• Boiling Point: 386.6°Cat760mmHg
• Flash Point: 182.1°C
• Appearance: /
• Density: 1.145g/cm³
• Vapor Pressure: 7.8E-06mmHg at 25°C
• Refractive Index: 1.628
• CAS DataBase Reference: chlorotriphenylethylene(CAS DataBase Reference)
• NIST Chemistry Reference: chlorotriphenylethylene(18084-97-4)
• EPA Substance Registry System: chlorotriphenylethylene(18084-97-4)

Safety Data

• Hazardous Substances Data: 18084-97-4(Hazardous Substances Data)

Usage

General Description

Chlorotriphenylethylene is a chemical compound with the molecular formula C20H15Cl. It is a chlorinated derivative of triphenylethylene, which is a synthetic organic compound. Chlorotriphenylethylene is used in organic synthesis as a building block for various pharmaceuticals and agrochemicals. It is also used as a ligand in metal-catalyzed reactions and as a precursor for the preparation of other organic compounds. This chemical is considered to be a potential endocrine disruptor due to its structural similarity to other compounds known to interfere with hormonal signaling in organisms. Its use and effects are closely monitored and regulated in various industries due to its potential environmental and health impacts.

InChI:InChI=1/C20H15Cl/c21-20(18-14-8-3-9-15-18)19(16-10-4-1-5-11-16)17-12-6-2-7-13-17/h1-15H

Upstream product

• 58-72-0 Triphenylethylene 
• 1733-63-7 1,2,2-triphenylethan-1-one 
• 42365-04-8 triphenylacetaldehyde 
• 109686-85-3 1,2-dichlorotriphenylethane 
• 119-61-9 benzophenone 
• 186968-62-7 2-(Chloro-phenyl-methyl)-5,5-dimethyl-[1,3,2]dioxaphosphinane 2-oxide 
• 10026-13-8 phosphorus pentachloride 
• 7782-50-5 chlorine 
• 64-19-7 acetic acid 
• 56-23-5 tetrachloromethane 
• 7791-25-5 sulfuryl dichloride 
• 94-36-0 dibenzoyl peroxide 
• 5271-39-6 Triphenylethan 
• 33885-01-7 1-chloro-2,2,2-triphenylethane 

Downstream Products

• 1520-42-9 1,1,2-triphenylethane 
• 119-61-9 benzophenone 
• 1040086-20-1 9-chloro-10-phenylphenanthrene 
• 56019-41-1 1-acetoxy-1,2,2-triphenylethene 
• 112349-27-6 9-acetoxy-10-phenylphenanthrene 
• 72989-40-3 buta-1,3-diene-1,1,2,3,4,4-hexaylhexabenzene 

Relevant articles and documents

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Reusable visible light photoredox catalysts; Catalyzed benzylic C(sp 3)-H functionalization/carbocyclization reactions

The C(sp3)-H functionalization/carbocyclization reaction through the oxidative quenching of visible light photoredox catalysts is established for constructing functionalized 1H-indenes. The process is general for a wide range of benzylic C(sps

Reactions on Aromatic Olefins Induced by Aminium Salts: Protic-Acid or Radical Cation Catalyzed Processes

Aromatic olefins by reaction with aminium salts lead, in strongly acidic reaction media, to different reaction products, arising from the intermediate formation of carbocation or radical-cation species.

Unsymmetrical Alkenes by Carbene Coupling from Diazirine Decomposition in the Presence of Diazo Compounds

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