10605-50-2

Basic information

• Product Name: Benzene, 1,1'-ethenylidenebis[3-chloro-
• CAS NO: 10605-50-2
• Molecular Formula: C14H10Cl2
• Molecular Weight: 249.139
• Mol File: 10605-50-2.mol
• Article Data: 5

Chemical Properties

• CAS DataBase Reference: Benzene, 1,1'-ethenylidenebis[3-chloro-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,1'-ethenylidenebis[3-chloro-(10605-50-2)
• EPA Substance Registry System: Benzene, 1,1'-ethenylidenebis[3-chloro-(10605-50-2)

Safety Data

• Hazardous Substances Data: 10605-50-2(Hazardous Substances Data)

Upstream product

• 141-78-6 ethyl acetate 
• 36229-42-2 (3-chlorophenyl)magnesium bromide 
• 7094-34-0 bis(3-chlorophenyl)methanone 
• 19493-09-5 Methylenetriphenylphosphorane 
• 1779-49-3 Methyltriphenylphosphonium bromide 
• 99-02-5 3'-Chloroacetophenone 

Downstream Products

• 138535-00-9 2,2-bis(3-chlorophenyl)ethanol 
• 138534-94-8 2,2-bis(m-chlorophenyl)ethyl tosylate 

Relevant articles and documents

Synergistic combination of visible-light photo-catalytic electron and energy transfer facilitating multicomponent synthesis of β-functionalized α,α-diarylethylamines

A synthetic strategy with the visible-light photo-catalytic synergistic combination of electron and energy transfer processes has been developed. The mild reaction conditions allow the radical-radical cross-coupling phenomenon for the multicomponent synthesis of β-arylsulfonyl(diarylphosphinoyl)-α,α-diarylethyl-amines from readily available arylsulfinic acids (diarylphosphine oxides), 1,1-diarylethylenes and arylazides.

Substituted 6,11-ethano-6,11-dihydrobenzo[b] quinolizinium salts and compositions and methods of use thereof

Substituted 6,11-ethano-6,11-dihydrobenzo[b]quinolizinium salts, pharmaceutical compositions containing them, and methods for the treatment of neurodegenerative disorders or neurotoxic injuries utilizing them, wherein the substituted 6,11-ethano-6,11-dihydrobenzo[b]quinolizinium salts have the formula: STR1 wherein: R1, R2, R3, R4, R5, R6, R7, X and p are as defined in the specification.

Substituent Effect Studies of Aryl-Assisted Solvolyses. I. The Acetolysis of 2,2-Bis(substituted phenyl)ethyl p-Toluenesulfonates

The substituent effect on the acetolysis of 2,2-bis(substituted phenyl)ethyl p-toluenesulfonates at 90.10 deg C can be described accurately in terms of the Yukawa-Tsuno (LArSR) relationship, giving a ρ value of -4.44 and an r value of 0.53. The substituent effect correlation of this system carrying two aryls is quite comparable to that of the 2-methyl-2-phenylpropyl system carrying a single aryl group, suggesting the close similarity in the structure of the transition states between the systems. The results can be reasonably accounted for on the basis of the accepted mechanism of this reaction, involving a rate-determining aryl-assisted transition state where only one aryl group of the two β-aryl groups participates.