3048-52-0

Usage

Uses

Used in Chemical Industry:
Benzene, 1,3,5-triethenylis used as a chemical intermediate for the manufacturing of polymers, resins, and specialty chemicals. Its reactivity makes it a valuable component in the synthesis of a wide range of organic compounds.
Used in Solvent Applications:
Due to its solubility properties, Benzene, 1,3,5-triethenylis used as a solvent in various chemical processes, facilitating reactions and improving the efficiency of production.
Used in Fragrance and Flavoring Industry:
Benzene, 1,3,5-triethenylis used as a component in the production of fragrances and flavoring agents, capitalizing on its sweet aroma to enhance the sensory qualities of various products.
However, it is important to note that Benzene, 1,3,5-triethenylis classified as a flammable substance and is considered a potential human carcinogen. Therefore, its use is regulated, and careful handling and storage are required to minimize potential health and environmental risks.

Upstream product

• 108-05-4 vinyl acetate 
• 626-39-1 1,3,5-trisbromobenzene 
• 7567-63-7 1,3,5-Triethynylbenzene 
• 18772-58-2 1,3,5-tris-(1-trimethylsilylethynyl)benzene 
• 779-90-8 1,3,5-triacetylbenzene 
• 7486-35-3 tri-n-butyl(vinyl)tin 
• 37394-26-6 α,α',α''-trimethyl-1,3,5-benzenetrimethanol 

Downstream Products

• 41009-81-8 1,3,5-Tris(2,2-dichlorcyclopropyl)benzol 
• 779-90-8 1,3,5-triacetylbenzene 
• 41009-73-8 1,3,5-Tris(1,2-dibromaethyl)benzol 

Relevant academic research and scientific papers

Nickel-Catalyzed Reductive Cross-Coupling of Aryl Bromides with Vinyl Acetate in Dimethyl Isosorbide as a Sustainable Solvent

A nickel-catalyzed reductive cross-coupling has been achieved using (hetero)aryl bromides and vinyl acetate as the coupling partners. This mild, applicable method provides a reliable access to a variety of vinyl arenes, heteroarenes, and benzoheterocycles, which should expand the chemical space of precursors to fine chemicals and polymers. Importantly, a sustainable solvent, dimethyl isosorbide, is used, making this protocol more attractive from the point of view of green chemistry.

NOVEL ANTIBIOTICS

Novel aryl compounds or pharmaceutically acceptable salts thereof, and uses of the same for the treatment of Gram-negative infections.

Tridentate Lewis Acids: Silicon-Functionalised 1,3,5-Triethynylbenzene and 1,3,5-Trivinylbenzene

Planar tridentate Lewis acids were synthesised by hydrosilylation reactions of triethynylbenzene with chlorosilanes. Hydrogenation of the rigid triethynylbenzene using hydrogen in the presence of Lindlar's catalyst resulted in the formation of trivinylben

SYNTHESIS OF ARYL COMPOUNDS

A method for the synthesis of a aryl compound of Formula (1). Formula (1)

Removal, recovery, and recycling of triarylphosphonium-supported tin reagents for various organic transformations

Phosphonium-supported tin reagents and catalysts were prepared and were shown to be effective in Stille couplings, radical dehalogenations, radical cyclizations, and carbonyl allylations. Not only could the tin residues be removed from the crude reaction mixture through a phase separation process but also they could be recovered and recycled.

New heck-type coupling reactions of natural tetrapyrroles - Synthesis of porphyrinoligomers bridged by divinyl- and trivinylbenzene

Using palladium(0)-catalyzed coupling reactions we were able to synthesize mono-, di-, and trimeric porphyrins linked by di- and trivinylbenzenes. The reactions were carried out with palladium(II) acetate in DMF under phase-transfer conditions. These coupling conditions are new in the field of porphyrin chemistry and proved to be a useful tool in the synthesis of C-C linked oligomeric porphyrins, as these compounds can be obtained in a simple one pot reaction with good yields.

Flash Pyrolysis of Selenides. Syntheses of Bibenzyls, Olefins, and Related Compounds

Pyrolyses of a series of selenides and diselenides were studied. Selenides and diselenides bound with an active methylene group like benzyl gave a variety of substituted bibenzyls and related ethane derivatives in high yields. Other diselenides were easily caused to cleave to give various aromatic and aliphatic olefins in good yields together with elemental selenium. Lepidopterene, paracyclophane, and benzocyclobutene were prepared by thermal cleavage of their corresponding phenylselenomethyl-substituted compounds as an application of the pyrolysis concerned.