2243-89-2

Basic information

• Product Name: 2,4,6-TRIMETHYLQUINOLINE
• Synonyms: 2,4,6-TRIMETHYLQUINOLINE;Trimethylquinoline
• CAS NO: 2243-89-2
• Molecular Formula: C₁₂H₁₃N
• Molecular Weight: 171.24
• EINECS: 218-823-0
• Mol File: 2243-89-2.mol
• Article Data: 7

Chemical Properties

• Melting Point: 68°C
• Boiling Point: 281.55°C
• Flash Point: 115.9 °C
• Appearance: /
• Density: 1.0420 (estimate)
• Vapor Pressure: 0.00594mmHg at 25°C
• Refractive Index: 1.6060 (estimate)
• CAS DataBase Reference: 2,4,6-TRIMETHYLQUINOLINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2,4,6-TRIMETHYLQUINOLINE(2243-89-2)
• EPA Substance Registry System: 2,4,6-TRIMETHYLQUINOLINE(2243-89-2)

Safety Data

• Hazardous Substances Data: 2243-89-2(Hazardous Substances Data)

Usage

General Description

2,4,6-Trimethylquinoline is a chemical compound that belongs to the class of quinoline derivatives. It is a yellowish-orange or brown crystalline solid with a faint, sweet odor. 2,4,6-TRIMETHYLQUINOLINE is used in the manufacture of dyes, pharmaceuticals, and rubber chemicals. It is also used as an intermediate in the production of other chemicals. Additionally, 2,4,6-Trimethylquinoline has been identified as an important component in petroleum products and has been used as an additive in motor oil to enhance its performance. It also has potential applications in the field of organic synthesis and materials science. Overall, 2,4,6-Trimethylquinoline is a versatile chemical with various industrial and research applications.

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

• 106-49-0 p-toluidine 
• 67-64-1 acetone 
• 74-86-2 acetylene 
• 7664-93-9 sulfuric acid 
• 56570-34-4 4-[(4-methylphenyl)amino]pent-3-en-2-one 
• 14353-69-6 N-mesityl-hydroxylamine 
• 625-33-2 3-penten-2-one 
• 83191-44-0 {4-methyl-2-[(2E)-1-methylbut-2-en-1-yl]phenyl}-amine 
• 7647-01-0 hydrogenchloride 
• 46387-10-4 1,2,2,4,6-pentamethyl-1,2-dihydroquinoline 
• 1810-78-2 2,2,4,6-tetramethyl-1,2-dihydroquinoline 
• 100161-85-1 4-Methyl-2-((E)-1-methyl-but-2-enyl)-phenylamine 
• 877-43-0 2,6-dimethylquinoline 
• 67-68-5 dimethyl sulfoxide 

Downstream Products

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

Relevant articles and documents

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

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.