2919-19-9

Usage

Uses

Used in Dye and Pigment Production:
1,1-DI(O-TOLYL)ETHYLENE is used as a chemical intermediate for the production of dyes and pigments, contributing to the development of colorants utilized in a wide range of industries.
Used in Pharmaceutical Synthesis:
In the pharmaceutical industry, 1,1-DI(O-TOLYL)ETHYLENE is utilized as an intermediate in the synthesis of various organic compounds, playing a crucial role in the creation of new medications and therapeutic agents.
Used in Polymer Stabilization:
1,1-DI(O-TOLYL)ETHYLENE is employed as a stabilizer in polymers, enhancing their durability and resistance to degradation, which is vital for the longevity and performance of plastic materials.
Used as a Reaction Initiator in Polymerization Processes:
This chemical compound also serves as a reaction initiator in polymerization processes, facilitating the formation of polymer chains and contributing to the advancement of polymer chemistry.
While 1,1-DI(O-TOLYL)ETHYLENE is considered to have low toxicity, it is essential to handle it with care, as exposure to high levels may result in skin, eye, and respiratory system irritation. Additionally, proper disposal and management are necessary to minimize its potential environmental impact.

InChI:InChI=1/C16H16/c1-12-8-4-6-10-15(12)14(3)16-11-7-5-9-13(16)2/h4-11H,3H2,1-2H3

Upstream product

• 932-31-0 ortho-tolylmagnesium bromide 
• 141-78-6 ethyl acetate 
• 75-36-5 acetyl chloride 
• 16419-60-6 2-Methylphenylboronic acid 
• 101640-66-8 1-(2-methylphenyl)ethenyl acetate 
• 38379-19-0 1-(1-chlorovinyl)-2-methylbenzene 
• 84109-17-1 2-methylphenylzinc chloride 
• 1093686-51-1 O,O-diethyl 1-o-tolylvinylphosphate 
• 577-16-2 2-Methylacetophenone 
• 1018-97-9 2,2'-dimethylbenzophenone 
• 75-16-1 methylmagnesium bromide 

Downstream Products

• 72853-76-0 4-Methyl-5-o-tolylbenzanthrachinone-7,12-dione 
• 33268-48-3 1,1-Di-o-tolyl-aethan 
• 118-90-1 ortho-methylbenzoic acid 
• 1018-97-9 2,2'-dimethylbenzophenone 

Relevant academic research and scientific papers

Synergistic combination of visible-light photo-catalytic electron and energy transfer facilitating multicomponent synthesis of β-functionalized α,α-diarylethylamines

A synthetic strategy with the visible-light photo-catalytic synergistic combination of electron and energy transfer processes has been developed. The mild reaction conditions allow the radical-radical cross-coupling phenomenon for the multicomponent synthesis of β-arylsulfonyl(diarylphosphinoyl)-α,α-diarylethyl-amines from readily available arylsulfinic acids (diarylphosphine oxides), 1,1-diarylethylenes and arylazides.

Selective cine substitution of 1-arylethenyl acetates with arylboron reagents and a diene/rhodium catalyst

When the crowd says Bo: A carbon-carbon bond is selectively formed at the β position of 1- arylethenyl acetate when the alkenyl substrate is reacted with arylboronic acids in the presence of a cycloocta-1,5-diene/rhodium catalyst. The choice of the ligand is crucial for the unusual cine substitution. Copyright

Studies on the 1,2-migrations in Pd-catalyzed negishi couplings with JosiPhos ligands

(Chemical Equation Presented) We report an initial investigation with the goal of determining the factors that control the 1,2-migration in the Negishi cross-coupling, which is promoted by palladium catalyst systems generated with JosiPhos ligands. Severa