48174-52-3

Basic information

• Product Name: Benzene, 1,1'-(1,2-ethanediyl)bis[4-ethenyl-
• CAS NO: 48174-52-3
• Molecular Formula: C18H18
• Molecular Weight: 234.341
• Mol File: 48174-52-3.mol
• Article Data: 6

Chemical Properties

• CAS DataBase Reference: Benzene, 1,1'-(1,2-ethanediyl)bis[4-ethenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,1'-(1,2-ethanediyl)bis[4-ethenyl-(48174-52-3)
• EPA Substance Registry System: Benzene, 1,1'-(1,2-ethanediyl)bis[4-ethenyl-(48174-52-3)

Safety Data

• Hazardous Substances Data: 48174-52-3(Hazardous Substances Data)

Usage

Description

Benzene, 1,1'-(1,2-ethanediyl)bis[4-ethenyl-, also known as diethylbenzene, is a colorless liquid with a sweet odor. It is a benzene derivative and is used as a solvent and intermediate in various chemical syntheses.

Uses

Used in Pharmaceutical Industry:
Benzene, 1,1'-(1,2-ethanediyl)bis[4-ethenylis used as a solvent for the synthesis of various pharmaceutical compounds. Its ability to dissolve a wide range of substances makes it a valuable component in the production of drugs.
Used in Plastics Industry:
In the plastics industry, Benzene, 1,1'-(1,2-ethanediyl)bis[4-ethenylserves as a solvent for the production of polymers. It helps in the processing and manufacturing of plastic materials, contributing to their desired properties.
Used in Rubber Manufacturing:
Benzene, 1,1'-(1,2-ethanediyl)bis[4-ethenylis utilized as a solvent in the rubber manufacturing process. It aids in the mixing and processing of rubber compounds, enhancing the production of rubber products.
Used as an Intermediate in Chemical Synthesis:
Benzene, 1,1'-(1,2-ethanediyl)bis[4-ethenylis used as an intermediate in the synthesis of various chemicals, including dyes, pharmaceuticals, and pesticides. Its role in these syntheses is crucial for the production of a wide range of chemical products.
It is important to handle Benzene, 1,1'-(1,2-ethanediyl)bis[4-ethenylwith care, as it is considered a hazardous material, and prolonged exposure may lead to adverse health effects.

Upstream product

• 103-29-7 1,1'-(1,2-ethanediyl)bisbenzene 
• 793-06-6 4,4'-diacetylbibenzyl 
• 38147-31-8 1,2-bis[4-(1-hydroxyethyl)phenyl]ethane 
• 1592-20-7 4-Vinylbenzyl chloride 
• 83352-47-0 bis(4-vinylphenylmethyl)sulfide 
• 142214-72-0 bis(4-vinylphenylmethyl)selenide 
• 87532-75-0 (4-vinylbenzyl)magnesium chloride 
• 2834-05-1 11-bromoundecanoic acid 

Relevant articles and documents

Catalytic synthesis of styryl-capped isotactic polypropylenes

Bis-styrenic molecules, 1,4-divinylbenzene (DVB) and 1,2-bis(4-vinylphenyl) ethane (BVPE), were successfully combined with hydrogen (H2) to form consecutive chain transfer complexes in propylene polymerization mediated by an isospecific metallocene catalyst (i.e., rac-dimethylsilylbis(2-methyl-4- phenylindenyl)zirconium dichloride, I) activated with methylaluminoxane (MAO), rendering a catalytic access to styryl-capped isotactic polypropylenes (i-PP). The chain transfer reaction took place in a unique way where prior to the ultimate chain transfer DVB/H2 or BVPE/H2 caused a copolymerizationlike reaction leading to the formation of main chain benzene rings. A preemptive polymer chain reinsertion was deduced after the consecutive actions of DVB/H2 or BVPE/H2, which gave the styryl-terminated polymer chain alongside a metal-hydride active species. It was confirmed that the chain reinsertion occurred in a regio-irregular 1,2-fashion, which contrasted with a normal 2,1-insertion of styrene monomer and ensured subsequent continuous propylene insertions, directing the polymerization to repeated DVB or BVPE incorporations inside polymer chain. Only as a competitive reaction, the insertion of propylene into metal-hydride site broke the chain propagation resumption process while completed the chain transfer process by releasing the styryl-terminated polymer chain. BVPE was found with much higher chain transfer efficiency than DVB, which was attributed to its non-conjugated structure with much divided styrene moieties resulting in higher polymerization reactivity but lower chain reinsertion tendency.

Synthetic method of 1,2-bis(4-vinylphenyl)ethane

The invention relates to a synthetic method of an organic intermediate, in particular to a synthetic method of 1,2-bis(4-vinylphenyl)ethane. A phase transfer catalysis method is adopted, p-chloromethyl styrene, copper powder and iron powder are used as raw materials, water and methylbenzene are used as solvents, and a phase transfer catalyst is added to synthesize the 1,2-bis(4-vinylphenyl)ethane.According to the synthetic method, the risk in the production process is low, the yield is improved, side reactions are reduced, and a high-quality product is obtained.

SYNTHESIS OF CYCLOBUTACYCLOPHANES CONTAINING GROUP 16 ELEMENTS BY INTRAMOLECULAR (2 ? + 2 ?) PHOTOCYCLOADDITION

The benzophenone-sensitized intramolecular (2 ? + 2 ?) photocycloaddition of bis(4-vinylphenylmethyl)sulfide and selenide in benzene afforded cyclobutacyclophanes containing sulfur and selenium in good yields.However, the photoreaction of bis(4-vinylpheny