18218-20-7

Basic information

• Product Name: 1-(1-(4-CHLOROPHENYL)VINYL)BENZENE
• Synonyms: 1-CHLORO-4-(1-PHENYL-VINYL)-BENZENE;1-(1-(4-CHLOROPHENYL)VINYL)BENZENE;1-Chloro-4-(1-phenylethenyl)benzene;1-Phenyl-1-(4-chlorophenyl)ethene;α-Phenyl-4-chlorostyrene;1-(4-Chlorophenyl)-1-phenylethene;1-Phenyl-1-(p-chlorophenyl)ethylene;EGIS 5926
• CAS NO: 18218-20-7
• Molecular Formula: C₁₄H₁₁Cl
• Molecular Weight: 214.69
• Mol File: 18218-20-7.mol
• Article Data: 64

Chemical Properties

• Boiling Point: 164 °C(Press: 16 Torr)
• Appearance: /
• Density: 1.107±0.06 g/cm3(Predicted)
• Refractive Index: 1.6115 (589.3 nm 28℃)
• Storage Temp.: 2-8°C
• CAS DataBase Reference: 1-(1-(4-CHLOROPHENYL)VINYL)BENZENE(CAS DataBase Reference)
• NIST Chemistry Reference: 1-(1-(4-CHLOROPHENYL)VINYL)BENZENE(18218-20-7)
• EPA Substance Registry System: 1-(1-(4-CHLOROPHENYL)VINYL)BENZENE(18218-20-7)

Safety Data

• Hazardous Substances Data: 18218-20-7(Hazardous Substances Data)

Usage

General Description

1-(1-(4-chlorophenyl)vinyl)benzene is a chemical compound with the molecular formula C16H13Cl. It is a derivative of benzene and is classified as an aryl vinyl compound. The compound consists of a benzene ring with a vinyl group and a 4-chlorophenyl group attached to it. It is commonly used in organic synthesis and as a building block for the construction of various organic compounds. Its chemical structure and properties make it a versatile intermediate in the production of various pharmaceuticals, agrochemicals, and fine chemicals. Additionally, it is also used as a fragrance ingredient in perfumes and in the production of specialty polymers.

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Downstream Products

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Relevant articles and documents

Electrochemical fluorosulfonylation of alkenes to access vicinal fluorinated sulfones derivatives

Herein, we report a practical and efficient fluorosulfonylation of the various alkenes with sulfonyl radical sources (RSO2NHNH2) and Et3N·3HF as cost-effective fluorination reagents under mild conditions. Remarkably, this

Photoinduced Hydroarylation and Cyclization of Alkenes with Luminescent Platinum(II) Complexes

Photoinduced hydroarylation of alkenes is an appealing synthetic strategy for arene functionalization. Herein, we demonstrated that aryl radicals generated from electron-deficient aryl chlorides/bromides could be trapped by an array of terminal/internal aryl alkenes in the presence of [Pt(O^N^C^N)] under visible-light (410 nm) irradiation, affording anti-Markovnikov hydroarylated compounds in up to 95 % yield. Besides, a protocol for [Pt(O^N^C^N)]-catalyzed intramolecular photocyclization of acrylanilides to give structurally diverse 3,4-dihydroquinolinones has been developed.

Electrochemistry enabled selective vicinal fluorosulfenylation and fluorosulfoxidation of alkenes

Both sulfur and fluorine play important roles in organic synthesis, the life science, and materials science. The direct incorporation of these elements into organic scaffolds with precise control of the oxidation states of sulfur moieties is of great significance. Herein, we report the highly selective electrochemical vicinal fluorosulfenylation and fluorosulfoxidation reactions of alkenes, which were enabled by the unique ability of electrochemistry to dial in the potentials on demand. Preliminary mechanistic investigations revealed that the fluorosulfenylation reaction proceeded through a radical-polar crossover mechanism involving a key episulfonium ion intermediate. Subsequent electrochemical oxidation of fluorosulfides to fluorosulfoxides were readily achieved under a higher applied potential with the adventitious H2O in the reaction mixture.