700-60-7

Basic information

• Product Name: (trichlorovinyl)benzene
• Synonyms: (trichlorovinyl)benzene;(Trichloroethenyl)benzene;Benzene,(1,2,2-trichloroethenyl)-
• CAS NO: 700-60-7
• Molecular Formula: C₈H₅Cl₃
• Molecular Weight: 207.4843
• EINECS: 211-848-8
• Mol File: 700-60-7.mol

Chemical Properties

• Boiling Point: 237.7 °C at 760 mmHg
• Flash Point: 148.8 °C
• Appearance: /
• Density: 1.372 g/cm³
• Vapor Pressure: 0.0679mmHg at 25°C
• Refractive Index: 1.583
• CAS DataBase Reference: (trichlorovinyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: (trichlorovinyl)benzene(700-60-7)
• EPA Substance Registry System: (trichlorovinyl)benzene(700-60-7)

Safety Data

• Hazardous Substances Data: 700-60-7(Hazardous Substances Data)

Usage

Uses

Used in Chemical Production:
(Trichlorovinyl)benzene is used as a solvent or in the production of other chemicals for various applications.
Used in Dye Industry:
(Trichlorovinyl)benzene is used as an intermediate in the manufacture of dyes, contributing to the development of colorants for various industries.
Used in Pharmaceutical Industry:
(Trichlorovinyl)benzene is used as an intermediate in the production of pharmaceuticals, aiding in the creation of medicinal compounds.
Used in Agricultural Chemical Industry:
(Trichlorovinyl)benzene is used as an intermediate in the manufacture of agricultural chemicals, playing a role in the development of products for crop protection and enhancement.
It is crucial to handle (trichlorovinyl)benzene with caution and adhere to proper safety measures during its use due to its hazardous nature.

InChI:InChI=1/C8H5Cl3/c9-7(8(10)11)6-4-2-1-3-5-6/h1-5H

Upstream product

• 618-34-8 1-chlorostyrene 
• 706-93-4 Phenylpentachloroethane 
• 127-18-4 1,1,2,2-tetrachloroethylene 
• 94-36-0 dibenzoyl peroxide 
• 960-71-4 triphenylborane 
• 3294-58-4 phenyl(bromodichloromethyl)mercury 
• 3141-47-7 (α,α-dichlorobenzyl)lithium 
• 71-43-2 benzene 
• 563-79-1 2,3-Dimethyl-2-butene 
• 139409-05-5 3-chloro-3-(α,α-dichlorobenzyl)diazirine 
• 86804-72-0 2,2-dichloro-1-phenylvinyl o-phenylene phosphite 
• 26788-89-6 phenylazo 4-methylphenyl sulfone 
• 4714-28-7 α,β,β,β-tetrachloroethylbenzene 
• 56-23-5 tetrachloromethane 

Downstream Products

• 4714-36-7 1-nitro-4-(1,2,2-trichlorovinyl)benzene 
• 713-33-7 (m-nitrophenyl)trichloroethylene 
• 103847-29-6 1-phenylethane-1,2,2-triphosphonic acid 
• 135340-54-4 (4-Bromomethyl-2,6-dichloro-phenyl)-(4-trichlorovinyl-phenyl)-methanone 
• 135340-70-4 5-Amino-1-[3,5-dichloro-4-(4-trichlorovinyl-benzoyl)-benzyl]-1H-[1,2,3]triazole-4-carboxylic acid amide 
• 730-50-7 N-<3-Trichlorvinyl-phenyl>-carbaminsaeureisopropylester 
• 63630-18-2 4(trichloroethenyl) o-nitroaniline 
• 60200-06-8 4-amino-6-trichlorovinyl-1,3-benzenedisulfonamide 
• 60285-85-0 4-amino-6-(trichlorovinyl)benzene-1,3-disulfonyl dichloride 
• 63630-20-6 2-Amino-4-(trichlorethenyl)benzolsulfonamid 
• 63630-17-1 4-(Trichlorethenyl)anilin 
• 135340-42-0 (2,6-Dichloro-4-methyl-phenyl)-(4-trichlorovinyl-phenyl)-methanone 
• 128080-48-8 cis-2-phenyl-1-tolyl-1,2-dichloroethene 
• 5216-32-0 cis-1,2-dichloro-1,2-diphenylethene 

Relevant articles and documents

THIOCYANATO-, BROMO-, AND CHLOROARYLATION OF TRICHLOROETHYLENE

By reactions of arenediazonium salts with trichloroethylene in aqueous acetone in the presence of alkali metal thiocyanates, bromides, or chlorides, catalyzed by Cu(II) or Fe(II) salts, we synthesized 1-thiocyanato(bromo, chloro)-1,2,2-trichloro-2-arylethanes.These were treated with alcoholic potassium hydroxide to give α,β,β-trichlorostyrenes.Trichloroethylene is less reactive in the anionarylation than vinylidene and vinyl chlorides.

Anomalous Michaelis-Becker Reaction: 1-Phenylethan-1,2,2-triphosphonic Acid and their Esters

Sodium dialkylphosphite reacts with trichlorovinylbenzene to yield in an one-batch procedure 1-phenyl-1,2,2-ethanetriphosphonic acid hexaalkyl esters.A carbanionic intermediate of an "anomalous Michaelis-Becker reaction" is deduced.Acidolysis of esters leads to the parent triphosphonic acids.NMR parameters of this acid are strongly influenced by protolytic equilibrium. - Key words: One-batch synthesis, Oligophosphonic Acid, NMR Spectra

CIDNP Studies of the Thermal Decomposition of Arylazo Aryl Sulfones

1H and 13C-CIDNP spectra were obtained during the thermal decomposition of several arylazo aryl sulfones (Ar-N=N-SO2-Ar') in tetrachloroethylene or 1,1,2,2-tetrachloroethane at 100 deg C.An enhanced absorption from the C1 of the starting material, azo sulfone, was observed; this indicates that the decomposition of azo sulfone proceeds by means of one-bond fission.The formation of sulfones (ArSO2Ar') and sulfinic esters (ArO(SO)Ar') as recombination products in a solvent cage was established from the signs of polarization (enhanced absorption or emission).