4541-89-3

Basic information

• Product Name: 1,1-Diphenyl-2-chloroethene
• Synonyms: 1,1'-(Chloroethenylidene)bisbenzene;1,1-Diphenyl-2-chloroethene
• CAS NO: 4541-89-3
• Molecular Formula: C₁₄H₁₁Cl
• Molecular Weight: 0
• Mol File: 4541-89-3.mol
• Article Data: 26

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 1,1-Diphenyl-2-chloroethene(CAS DataBase Reference)
• NIST Chemistry Reference: 1,1-Diphenyl-2-chloroethene(4541-89-3)
• EPA Substance Registry System: 1,1-Diphenyl-2-chloroethene(4541-89-3)

Safety Data

• Hazardous Substances Data: 4541-89-3(Hazardous Substances Data)

Upstream product

• 119-61-9 benzophenone 
• 5293-84-5 chloromethyltriphenylphosphonium chloride 
• 244028-13-5 2,2-diphenylmethylchlorocarbene radical 
• 1210-39-5 3,3-diphenyl-2-propenal 
• 606-84-8 3,3-diphenylacrylic acid 
• 135-19-3 β-naphthol 
• 209391-60-6 [2-chloro-2-(p-tolylsulfinyl)ethene-1,1-diyl]dibenzene 
• 7529-42-2 AgCClC(C₆H₅)2 
• 209391-91-3 2-Chloro-1,1-diphenyl-2-(toluene-4-sulfinyl)-ethanol 
• 13249-58-6 1-bromo-2,2-diphenylethylene 
• 67-66-3 chloroform 
• 59856-00-7 1,2-dichloro-1,1-diphenylethane 
• 2779-69-3 1,1-dichloro-2,2-diphenylethene 
• 599-67-7 1,1-diphenylethanol 

Downstream Products

• 36586-15-9 (2-ethoxyethene-1,1-diyl)dibenzene 
• 501-65-5 diphenyl acetylene 
• 63002-14-2 1,2,2-trichloro-1,1-diphenyl-ethane 
• 4359-35-7 2-diphenylmethyl-1,3-dioxolane 
• 101119-31-7 1-acetoxy-2,2-dichloro-1,1-diphenylethane 
• 4541-88-2 α-Chlor-β.β-diphenyl-acrylsaeure 
• 19937-32-7 Bis-<1-chlor-2,2-diphenyl-vinyl>-keton 
• 69036-00-6 1-chloro-2,2-diphenyl-1-(trimethylsilyl)ethene 
• 37916-93-1 2-Chlor-4,5-dibrom-1,1-diphenyl-pentan 
• 38185-93-2 2-Chlor-1-methoxy-3,3-diphenyl-propen-⁽²⁾ 
• 19937-41-8 4-Chlor-2-cyan-3.3.5.5-tetraphenyl-penten-⁽⁴⁾-saeure-nitril 
• 38185-94-3 2-chloro-1,3,3-triphenylprop-2-en-1-one 
• 950-79-8 β-Chlor-β-brom-α,α-diphenylethylen 
• 5293-63-0 1-Chlor-1-iod-2,2-diphenylethylen 

Relevant articles and documents

Copper(i)-catalyzed radical carboamination reaction of 8-aminoquinoline-oriented buteneamides with chloroform: synthesis of-β-lactams

A novel Cu(CH3CN)4PF6-catalyzed carboamination reaction of 8-aminoquinoline-oriented buteneamides with chloroform to afford 4-(2,2,2-trichloroethyl)-β-lactams is described. The reaction proceeded at 110 °C in air with di-t

Visible light-mediated metal-free double bond deuteration of substituted phenylalkenes

Various bromophenylalkenes were reductively photodebrominated by using 1,3-dimethyl-2-phenyl-1H-benzo-[d]imidazoline (DMBI) and 9,10-dicyanoanthracene. With deuterated DMBI analogs (the most effective was DMBI-d11), satisfactory to excellent isotopic yields were obtained. DMBI-d11 could also be regenerated from the reaction mixtures with a recovery rate of up to 50%. The combination of the photodebromination reaction with conventional methods for bromoalkene synthesis enables sequential monodeuteration of a double bond without the necessity of a metal catalyst. This journal is

Halogenation of 1,1-diarylethylenes by N-halosuccinimides

An efficient method for the preparation of 2,2-diarylvinyl halides from the corresponding 1,1-diarylethylenes has been developed. N-Halosuccinimides (N-bromosuccinimide or N-chlorosuccinimide) were used as the halogenation reagents. The practicability of this method is highlighted by its simple operation, broad substrate scope and capability for large-scale reaction.