3883-13-4

Basic information

• Product Name: (2,2,2-Trichloroethyl)benzene
• Synonyms: (2,2,2-Trichloroethyl)benzene
• CAS NO: 3883-13-4
• Molecular Formula: C₈H₇Cl₃
• Molecular Weight: 0
• Mol File: 3883-13-4.mol
• Article Data: 8

Chemical Properties

• Appearance: /
• CAS DataBase Reference: (2,2,2-Trichloroethyl)benzene(CAS DataBase Reference)
• NIST Chemistry Reference: (2,2,2-Trichloroethyl)benzene(3883-13-4)
• EPA Substance Registry System: (2,2,2-Trichloroethyl)benzene(3883-13-4)

Safety Data

• Hazardous Substances Data: 3883-13-4(Hazardous Substances Data)

Usage

General Description

(2,2,2-Trichloroethyl)benzene is a chemical compound that consists of a benzene ring with a trichloroethyl group attached to it. It is a colorless liquid with a very strong odor. This chemical is primarily used as an intermediate in the production of various chemicals such as dyes, pigments, and pharmaceuticals. It is also used as a solvent for cellulose ethers, oils, and resins. However, (2,2,2-Trichloroethyl)benzene is considered to be a hazardous substance, as it has been shown to have toxic effects on the environment and human health. It is listed as a hazardous air pollutant and a hazardous waste in some regions. Therefore, its use and disposal should be carefully managed to minimize its impact on the environment and human health.

Upstream product

• 67-66-3 chloroform 
• 100-44-7 benzyl chloride 
• 2547-61-7 Trichloromethanesulfonyl chloride 
• 75-62-7 Bromotrichloromethane 
• 100-51-6 benzyl alcohol 
• 56-23-5 tetrachloromethane 
• 68307-67-5 2-chloro[(trimethylsilyl)methyl]benzene 
• 17876-99-2 (4-chlorobenzyl)trimethylsilane 
• 75-35-4 1,1-Dichloroethylene 
• 100-34-5 benzene diazonium chloride 
• 100-39-0 benzyl bromide 
• 108-88-3 toluene 
• 41139-88-2 Phenylacetyl-triphenylsilan 
• 53617-91-7 C₁₁H₁₉N₂OP 

Downstream Products

• 698-88-4 (2,2-dichlorovinyl)benzene 
• 4412-39-9 (2,2-dichloroethyl)benzene 
• 104415-94-3 1-Butyl-3-chloro-1,4-dihydro-naphthalene 
• 104415-91-0 (2,2,4-Trichloro-octyl)-benzene 
• 104415-93-2 1-Butyl-3-chloro-1,2-dihydro-naphthalene 
• 104415-96-5 2-chloro-1-phenyl-1,3-octadiene 
• 104415-95-4 ((E)-2,4-Dichloro-oct-1-enyl)-benzene 
• 104415-89-6 1-Butyl-3,3-dichloro-1,2,3,4-tetrahydro-naphthalene 
• 139489-24-0 (2,2-Dichloro-2-thiocyanato-ethyl)-benzene 
• 32092-99-2 1-methyl-4-(3-phenylpropa-1,2-dienyl)benzene 
• 1669-54-1 (E)-1-(4-methylphenyl)-3-phenyl-2-propen-1-ol 
• 1190230-33-1 (E)-2-benzylidene-1-(5-(tert-butyldiphenylsilyloxy)pentyl)cyclobutanol 
• 1190230-31-9 (E)-2-benzylidene-1-pentylcyclobutanol 
• 1190230-40-0 (E)-8-benzylidenebicyclo[4.2.0]octan-1-ol 

Relevant articles and documents

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A convenient synthesis of (Z)-1-chloro-1-alkenes and (Z)-1-chloro-2-alkoxy-1-alkenes

Mild, room temperature CrCl2 reduction of 1,1,1-trichloroalkanes stereoselectively generates (Z)-1-chloro-2-substituted-1-alkenes in excellent yields.

ABSOLUTE RATES AND SELECTIVITY OF HOMOLYTIC SUBSTITUTION AT A CARBON ATOM IN BENZYL COMPLEXES OF COBALT. EFFECT OF AXIAL LIGANDS

The absolute rate constants were determined for the bimolecular homolytic substitution of organocobalt groups by a trichloromethyl radical in the benzylglyoxime complexes of cobalt, and the effect of axial and equatorial ligands on the reaction rate was studied.The change in the dissociation energy of the cobalt-carbon bond has a determining effect on the substitution rate.The relation between the reactivity and selectivity with variation of the axial ligand is inverse in nature.