2243-89-2

Usage

Uses

Used in Chemical Production:
2,4,6-Trimethylquinoline is used as an intermediate in the production of other chemicals, contributing to the synthesis of a range of compounds.
Used in Dye Industry:
2,4,6-Trimethylquinoline is used as a component in the manufacture of dyes, providing color and stability to various products.
Used in Pharmaceutical Industry:
2,4,6-Trimethylquinoline is utilized in the production of pharmaceuticals, playing a role in the development of new drugs and medications.
Used in Rubber Chemical Industry:
2,4,6-Trimethylquinoline is employed in the manufacture of rubber chemicals, enhancing the properties and performance of rubber products.
Used in Petroleum Products:
2,4,6-Trimethylquinoline has been identified as an important component in petroleum products, particularly as an additive in motor oil to improve its performance.
Used in Organic Synthesis and Materials Science:
2,4,6-Trimethylquinoline has potential applications in the field of organic synthesis and materials science, contributing to the development of new materials and compounds.

InChI:InChI=1/C12H13N/c1-8-4-5-12-11(6-8)9(2)7-10(3)13-12/h4-7H,1-3H3

Upstream product

• 1810-78-2 2,2,4,6-tetramethyl-1,2-dihydroquinoline 
• 56570-34-4 4-[(4-methylphenyl)amino]pent-3-en-2-one 
• 106-49-0 p-toluidine 
• 107-21-1 ethylene glycol 
• 67-64-1 acetone 
• 540-23-8 p-toluidine hydrochloride 
• 74-86-2 acetylene 
• 123-54-6 acetylacetone 
• 123-63-7 paracetaldehyde 
• 67-68-5 dimethyl sulfoxide 
• 877-43-0 2,6-dimethylquinoline 
• 100161-85-1 4-Methyl-2-((E)-1-methyl-but-2-enyl)-phenylamine 
• 7647-01-0 hydrogenchloride 
• 46387-10-4 1,2,2,4,6-pentamethyl-1,2-dihydroquinoline 

Downstream Products

• 22932-62-3 4-benzoyloxy-2,4,6-trimethyl-cyclohexa-2,5-dienone 
• 5431-69-6 N,N-diethyl-4-[trans-2-(4,6-dimethyl-[2]quinolyl)-vinyl]-aniline 
• 5442-96-6 4,6-dimethyl-2-(p-N,N-dimethylaminostyryl)quinoline 
• 651733-52-7 2,4,6-trimethyl-5,6,7,8-tetrahydro-quinoline 
• 123636-86-2 (S)-2-{4-[(2,4-Dimethyl-quinolin-6-ylmethyl)-prop-2-ynyl-amino]-benzoylamino}-pentanedioic acid 

Relevant academic research and scientific papers

Cyclization of ortho-(alk-2-enyl) anilines under the action of iodine

The reaction of ortho-(cyclohex-2-enyl)aniline with I2 in nonpolar and polar solvents affords predominantly 1-iodohexahydrocarbazole and azatricyclotridecatriene, respectively. Under analogous conditions, 4-methyl-2-(1-methylbut-2-en-l-yl)anili

Miceller-mediated phosphomolybdic acid: Highly effective reusable catalyst for synthesis of quinoline and its derivatives

A simple, efficient, and ecofriendly procedure has been developed for the synthesis of quinoline and its derivatives in a one-pot reaction of aniline with crotonaldehyde or methyl vinyl ketone using phosphomolybdic acid as solid acid catalyst in miceller media. The catalyst was easily recycled and reused. Copyrigh

Reactions of N- and C-alkenylanilines: III. Synthesis and cyclization of substituted 2-(1-methyl-2-butenyl)anilines

Reactions of substituted 2-(1-methyl-2-butenyl)anilines with iodine result in cyclization and formation of 3-iodo-1,2,3,4-tetrahydroquinolines; N-methylsulfonyl-2-(1-methyl-2-butenyl)anilines give rise exclusively to the corresponding 2-(1-iodoethyl)-3-methyl-2,3-dihydroindoles.

Synthesis of substituted pyrrolo[1,2-a]quinolines

5, 7-Dimethyl-2-(phenyl or 4′-substituted phenyl)pyrrolo[1, 2-a)quinolines (6-10) have been synthesised by the reaction of 2,4,6-trimethylquinoline with phenacyl bromide and/or 4-substituted phenacyl bromide. These compounds have been characterised through their PMR spectral analysis.

INTRAMOLECULAR CATALYTIC CYCLIZATION OF SUBSTITUTED 2-ALKENYLANILINES

A study was carried out on the effect of the nature and structure of the substituent in the aromatic ring of 2-(1-methyl-2-butenyl)anilines on the direction and structural selectivity of the their intramolecular cyclization to derivatives of quinoline and indole by the action of catalytic amounts of PdCl2 or PdCl2-(DMSO)n complexes.