3048-52-0

Basic information

• Product Name: Benzene, 1,3,5-triethenyl-
• CAS NO: 3048-52-0
• Molecular Formula: C12H12
• Molecular Weight: 156.227
• Mol File: 3048-52-0.mol
• Article Data: 7

Chemical Properties

• CAS DataBase Reference: Benzene, 1,3,5-triethenyl-(CAS DataBase Reference)
• NIST Chemistry Reference: Benzene, 1,3,5-triethenyl-(3048-52-0)
• EPA Substance Registry System: Benzene, 1,3,5-triethenyl-(3048-52-0)

Safety Data

• Hazardous Substances Data: 3048-52-0(Hazardous Substances Data)

Usage

General Description

Benzene, 1,3,5-triethenyl, also known as symmetrical tri-ethenylbenzene, is a chemical compound with the molecular formula C12H10. It is a colorless to light yellow liquid with a sweet aroma and is used as a chemical intermediate in the production of various organic compounds. 1,3,5-triethenylbenzene is primarily used in the manufacturing of polymers, resins, and specialty chemicals. It is also used as a solvent and as a component in the production of fragrances and flavoring agents. Benzene, 1,3,5-triethenyl- is known for its reactivity and is classified as a flammable substance, requiring careful handling and storage. Additionally, it is considered a potential human carcinogen and its use is regulated to minimize potential health and environmental risks.

Upstream product

• 626-39-1 1,3,5-trisbromobenzene 
• 108-05-4 vinyl acetate 
• 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 
• 7567-63-7 1,3,5-Triethynylbenzene 
• 18772-58-2 1,3,5-tris-(1-trimethylsilylethynyl)benzene 

Downstream Products

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

Relevant articles and documents

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.

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.