Cas no 88565-88-2 (4,6,8-Trimethylquinoline)

4,6,8-Trimethylquinoline is a substituted quinoline derivative characterized by its three methyl groups at the 4, 6, and 8 positions. This compound is valued for its role as an intermediate in organic synthesis, particularly in the production of pharmaceuticals, agrochemicals, and specialty chemicals. Its structural features contribute to enhanced stability and reactivity, making it suitable for applications requiring selective functionalization. The methyl groups influence electronic and steric properties, facilitating tailored modifications in complex molecular frameworks. 4,6,8-Trimethylquinoline is typically supplied as a high-purity solid or liquid, ensuring consistency in research and industrial processes. Its utility in heterocyclic chemistry underscores its importance in advanced synthetic methodologies.
4,6,8-Trimethylquinoline structure
4,6,8-Trimethylquinoline structure
Product Name:4,6,8-Trimethylquinoline
CAS No:88565-88-2
MF:C12H13N
MW:171.238322973251
MDL:MFCD00191505
CID:709818
PubChem ID:87577175
Update Time:2025-05-28

4,6,8-Trimethylquinoline Chemical and Physical Properties

Names and Identifiers

    • Quinoline,4,6,8-trimethyl-
    • 4,6,8-Trimethylquinoline
    • 4,6,8-Trimethyl-chinolin
    • 4,6,8-trimethyl-quinoline
    • 4,6,8-Trimethylquinoline1000μg
    • Quinoline,4,6,8-trimethyl
    • 4,6,8-Trimethylquinoline (ACI)
    • CHEMBL2135849
    • SCHEMBL4513038
    • AKOS015842639
    • DTXSID80659954
    • T1409
    • NCGC00188239-01
    • 88565-88-2
    • CS-0326094
    • T73038
    • SB67503
    • MFCD00191505
    • AC-27932
    • MDL: MFCD00191505
    • Inchi: 1S/C12H13N/c1-8-6-10(3)12-11(7-8)9(2)4-5-13-12/h4-7H,1-3H3
    • InChI Key: HNCYZWOTJQPKTQ-UHFFFAOYSA-N
    • SMILES: N1C2C(=CC(C)=CC=2C)C(C)=CC=1

Computed Properties

  • Exact Mass: 171.10500
  • Monoisotopic Mass: 171.104799419g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 1
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 0
  • Complexity: 178
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 12.9
  • Surface Charge: 0
  • Tautomer Count: nothing
  • XLogP3: 3.3

Experimental Properties

  • Color/Form: Not determined
  • Melting Point: 56.0 to 60.0 deg-C
  • PSA: 12.89000
  • LogP: 3.16000
  • Solubility: Not determined

4,6,8-Trimethylquinoline Security Information

4,6,8-Trimethylquinoline Customs Data

  • HS CODE:2933499090
  • Customs Data:

    China Customs Code:

    2933499090

    Overview:

    2933499090. Other compounds containing quinoline or isoquinoline ring system [but not further fused]. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date

    Summary:

    2933499090. other compounds containing in the structure a quinoline or isoquinoline ring-system (whether or not hydrogenated), not further fused. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

4,6,8-Trimethylquinoline Pricemore >>

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4,6,8-Trimethylquinoline Production Method

Production Method 1

Reaction Conditions
1.1 Reagents: Zinc chloride Solvents: Ethanol ,  Water ;  0.5 h, 40 °C
1.2 Reagents: Iron chloride (FeCl3) ;  1 h, 40 °C → 80 °C; 15 h, 80 °C; 80 °C → rt
1.3 Reagents: Sodium hydroxide Solvents: Water
Reference
Photoredox Neutral Decarboxylative Hydroxyalkylations of Heteroarenes with α-Keto Acids
Ji, Xiaochen ; Yang, Zhonglin; Wu, Xinzhuang; Deng, Guo-Jun ; Huang, Huawen, Journal of Organic Chemistry, 2022, 87(6), 4168-4182

4,6,8-Trimethylquinoline Raw materials

4,6,8-Trimethylquinoline Preparation Products

4,6,8-Trimethylquinoline Suppliers

Amadis Chemical Company Limited
Gold Member
Audited Supplier Audited Supplier
(CAS:88565-88-2)4,6,8-Trimethylquinoline
Order Number:A1207343
Stock Status:in Stock
Quantity:1g
Purity:99%
Pricing Information Last Updated:Monday, 2 September 2024 15:57
Price ($):158.0

Additional information on 4,6,8-Trimethylquinoline

Recent Advances in the Study of 4,6,8-Trimethylquinoline (CAS: 88565-88-2) in Chemical Biology and Pharmaceutical Research

4,6,8-Trimethylquinoline (CAS: 88565-88-2) is a quinoline derivative that has garnered significant attention in recent years due to its potential applications in chemical biology and pharmaceutical research. This compound, characterized by its unique structural features, has been the subject of numerous studies aimed at exploring its biological activities, synthetic pathways, and therapeutic potential. The following sections provide a comprehensive overview of the latest research findings related to 4,6,8-Trimethylquinoline, highlighting its significance in the field.

Recent studies have focused on the synthesis and structural modification of 4,6,8-Trimethylquinoline to enhance its biological activity. Researchers have developed novel synthetic routes to produce this compound with high yield and purity, which is critical for its application in drug discovery. Advanced spectroscopic techniques, including NMR and mass spectrometry, have been employed to confirm the structure and purity of the synthesized compound. These efforts have paved the way for further investigations into its pharmacological properties.

One of the most promising aspects of 4,6,8-Trimethylquinoline is its potential as an antimicrobial agent. In vitro studies have demonstrated its efficacy against a range of bacterial and fungal pathogens, including drug-resistant strains. The compound's mechanism of action appears to involve disruption of microbial cell membranes and inhibition of essential enzymatic processes. These findings suggest that 4,6,8-Trimethylquinoline could serve as a lead compound for the development of new antimicrobial therapies, particularly in the face of rising antibiotic resistance.

In addition to its antimicrobial properties, 4,6,8-Trimethylquinoline has shown promise in anticancer research. Preliminary studies indicate that the compound exhibits selective cytotoxicity against certain cancer cell lines, while sparing normal cells. Researchers are investigating its potential to induce apoptosis and inhibit angiogenesis, which are critical processes in cancer progression. These studies are still in the early stages, but the results are encouraging and warrant further exploration.

The pharmacokinetic and toxicological profiles of 4,6,8-Trimethylquinoline are also under investigation. Understanding these aspects is essential for assessing the compound's suitability as a drug candidate. Recent preclinical studies have provided valuable insights into its absorption, distribution, metabolism, and excretion (ADME) properties, as well as its safety profile. These data will be crucial for guiding future clinical trials and optimizing the compound's therapeutic potential.

In conclusion, 4,6,8-Trimethylquinoline (CAS: 88565-88-2) represents a promising area of research in chemical biology and pharmaceutical science. Its diverse biological activities, coupled with advances in synthetic chemistry, make it a valuable candidate for further development. Ongoing studies are expected to uncover new applications and refine its therapeutic potential, contributing to the advancement of medicine and healthcare.

Recommended suppliers
Amadis Chemical Company Limited
(CAS:88565-88-2)4,6,8-Trimethylquinoline
A1207343
Purity:99%
Quantity:1g
Price ($):158.0
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