384-65-6

Basic information

• Product Name: Benzene, (1-chloro-2,2,2-trifluoroethyl)-
• CAS NO: 384-65-6
• Molecular Formula: C8H6ClF3
• Molecular Weight: 194.584
• Mol File: 384-65-6.mol
• Article Data: 11

Chemical Properties

• CAS DataBase Reference: Benzene, (1-chloro-2,2,2-trifluoroethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, (1-chloro-2,2,2-trifluoroethyl)-(384-65-6)
• EPA Substance Registry System: Benzene, (1-chloro-2,2,2-trifluoroethyl)-(384-65-6)

Safety Data

• Hazardous Substances Data: 384-65-6(Hazardous Substances Data)

Upstream product

• 771-61-9 2,3,4,5,6-pentafluorophenol 
• 60988-78-5 α-trifluoromethylbenzyl dichlorophosphate 
• 340-03-4 2-chloro-2,2-difluoro-1-phenyl-ethan-1-ol 
• 434-44-6 1,2-dichloro-1-phenyl-2,2-difluoroethane 
• 340-04-5 1-phenyl-2,2,2-trifluoromethylethanol 
• 340-06-7 S(+)-1-phenyl-2,2,2-trifluoroethanol 
• 433-27-2 ethyl trifluoroacetaldehyde hemiacetal 
• 71-43-2 benzene 
• 58852-20-3 α-Chlor-α-Tritio-β,β,β-trifluoraethylbenzol 
• 78844-54-9 α-Chlor-α-Deutero-β,β,β-trifluoraethylbenzol 
• 124-41-4 sodium methylate 
• 2787-79-3 4-Trifluoromethyl-2,3,5,6-tetrafluorophenol 
• 394-98-9 α-chloro-β,β-difluorostyrene 
• 21249-93-4 (2,2,2-trifluoroethyl)benzene 

Downstream Products

• 78844-54-9 α-Chlor-α-Deutero-β,β,β-trifluoraethylbenzol 
• 394-98-9 α-chloro-β,β-difluorostyrene 
• 21249-93-4 (2,2,2-trifluoroethyl)benzene 
• 384-63-4 (1,2-dibromo-2,2-difluoro-ethyl)-benzene 
• 405-42-5 2',2'-difluorostyrene 
• 2925-57-7 1-chloro-1-(3-trifluoromethylphenyl)-2,2,2-trifluoroethane 
• 128408-39-9 C₈H₆F₃⁽¹⁺⁾ 
• 191402-60-5 1-(1-Chloro-2,2,2-trifluoro-ethyl)-4-trifluoromethyl-benzene 
• 191402-51-4 5-(1-Chloro-2,2,2-trifluoro-ethyl)-2-methoxy-benzonitrile 
• 81577-13-1 1-(1-Chloro-2,2,2-trifluoro-ethyl)-4-fluoro-benzene 
• 708-65-6 1-chloro-1-(4-methylphenyl)-2,2,2-trifluoroethane 
• 191402-55-8 1-(1-Chloro-2,2,2-trifluoro-ethyl)-3-methyl-benzene 

Relevant articles and documents

Stille cross-coupling of secondary and tertiary α-(trifluoromethyl)-benzyl chlorides with allylstannanes

A Stille cross-coupling reaction was developed that delivers for the first time trifluoromethyl-substituted homoallyl compounds from α-(trifluoromethyl)benzyl chlorides and allylstannanes. This reaction proceeds even with low catalyst loadings (1 mol%) vi

Fungicidal compounds having a fluorovinyl-or fluoropropenyl-oxyphenyloxime moiety and process for the preparation thereof

A fungicidal compound of formula (I) having a fluorovinye- or fluoropropenyl-oxyphenyloxime moiety and stereoisomers thereof are useful for protecting crops from fungal diseases: wherein, X is CH or N; Y is O or NH; R1is hydrogen, C1-4alkyl, or halogen-substituted C1-4alkyl, R2is a phenyl group optionally carrying one or more substituents selected from the group consisting of C1-4alkyl, C1-4alkoxy, methylenedioxy and halogen; or a naphthyl group; and R3is hydrogen or CF3.

Catalytic phosphorylation of polyfluoroalkanols 17. * Synthesis and the stereochemistry of tris(α-trifluoromethylbenzyl) phosphates

Catalytic phosphorylation of α-trifluoromethylbenzyl alcohols with POCl3 taken in a ratio of 3 : 1 under particular temperature conditions afforded predominantly symmetrical tris(α-trifluoromethylbenzyl) phosphates. The latter were obtained as mixtures of two diastereomers with a statistical ratio of the components.