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
• Article Data: 5

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

General Description

(trichlorovinyl)benzene is a chemical compound with the molecular formula C8H5Cl3. It is a colorless liquid at room temperature and is insoluble in water. This chemical is primarily used as a solvent or in the production of other chemicals. It is also used as an intermediate in the manufacture of dyes, pharmaceuticals, and agricultural chemicals. However, (trichlorovinyl)benzene is considered to be a hazardous substance, as it is a skin and eye irritant, and prolonged exposure can cause respiratory and skin sensitization. It is important to handle this chemical with caution and follow proper safety precautions during its use.

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 
• 2870-30-6 sodium diethyl phosphate 
• 103808-48-6 1-Phenylethan-1,2,2-trisphosphonsaeurehexaethylester 
• 103808-47-5 1-Phenylethan-1,2,2-trisphosphonsaeurehexaisopropylester 
• 5216-32-0 cis-1,2-dichloro-1,2-diphenylethene 
• 128080-48-8 cis-2-phenyl-1-tolyl-1,2-dichloroethene 
• 135340-42-0 (2,6-Dichloro-4-methyl-phenyl)-(4-trichlorovinyl-phenyl)-methanone 
• 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 
• 63630-17-1 4-(Trichlorethenyl)anilin 
• 63630-20-6 2-Amino-4-(trichlorethenyl)benzolsulfonamid 
• 60285-85-0 4-amino-6-(trichlorovinyl)benzene-1,3-disulfonyl dichloride 

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).