Cas no 92513-34-3 (2,7,8-Trimethylquinoline-3-carboxylic Acid)

2,7,8-Trimethylquinoline-3-carboxylic Acid structure
92513-34-3 structure
Product Name:2,7,8-Trimethylquinoline-3-carboxylic Acid
CAS No:92513-34-3
MF:C13H13NO2
MW:215.247823476791
MDL:MFCD08437591
CID:891664
PubChem ID:329773387
Update Time:2025-04-23

2,7,8-Trimethylquinoline-3-carboxylic Acid Chemical and Physical Properties

Names and Identifiers

    • 2,7,8-TRIMETILQUINOLINE-3-CARBOXYLIC ACID
    • 2,7,8-TRIMETHYLQUINOLINE-3-CARBOXYLIC ACID
    • 7,8-Dimethylquinaldine-3-carboxylic acid
    • QU148
    • 2,7,8-Trimethylquinoline-3-carboxylic acid, AldrichCPR
    • 92513-34-3
    • MFCD08437591
    • DTXSID30588902
    • AB45161
    • CS-0458063
    • 2,7,8-Trimethylquinoline-3-carboxylic Acid
    • MDL: MFCD08437591
    • Inchi: 1S/C13H13NO2/c1-7-4-5-10-6-11(13(15)16)9(3)14-12(10)8(7)2/h4-6H,1-3H3,(H,15,16)
    • InChI Key: KNGACCJHYQQKRJ-UHFFFAOYSA-N
    • SMILES: OC(C1=C(C)N=C2C(C=CC(C)=C2C)=C1)=O

Computed Properties

  • Exact Mass: 215.09500
  • Monoisotopic Mass: 215.094628657g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 16
  • Rotatable Bond Count: 1
  • Complexity: 279
  • 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
  • XLogP3: 2.8
  • Topological Polar Surface Area: 50.2?2

Experimental Properties

  • Density: 1.2±0.1 g/cm3
  • Boiling Point: 375.0±37.0 °C at 760 mmHg
  • Flash Point: 180.6±26.5 °C
  • PSA: 50.19000
  • LogP: 2.85820
  • Vapor Pressure: 0.0±0.9 mmHg at 25°C

2,7,8-Trimethylquinoline-3-carboxylic Acid Security Information

  • Symbol: GHS07
  • Signal Word:Warning
  • Hazard Statement: H302-H319
  • Warning Statement: P305+P351+P338
  • Hazardous Material transportation number:NONH for all modes of transport
  • WGK Germany:3
  • Hazard Category Code: 22-36
  • Safety Instruction: 26
  • Hazardous Material Identification: Xn
  • Storage Condition:storage at -4℃ (1-2weeks), longer storage period at -20℃ (1-2years)

2,7,8-Trimethylquinoline-3-carboxylic Acid Pricemore >>

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Additional information on 2,7,8-Trimethylquinoline-3-carboxylic Acid

Exploring the Versatile Applications and Properties of 2,7,8-TRIMETILQUINOLINE-3-CARBOXYLIC ACID (CAS No. 92513-34-3)

2,7,8-TRIMETILQUINOLINE-3-CARBOXYLIC ACID (CAS No. 92513-34-3) is a specialized organic compound that has garnered significant attention in the fields of pharmaceuticals, agrochemicals, and material science. This quinoline derivative is known for its unique structural properties, which make it a valuable intermediate in the synthesis of various bioactive molecules. Researchers and industry professionals are increasingly interested in this compound due to its potential applications in drug development and advanced material engineering.

The molecular structure of 2,7,8-TRIMETILQUINOLINE-3-CARBOXYLIC ACID features a quinoline core with three methyl groups at positions 2, 7, and 8, along with a carboxylic acid functional group at the 3-position. This configuration imparts distinct chemical reactivity, making it a versatile building block for synthesizing complex molecules. The presence of the carboxylic acid group allows for further derivatization, enabling the creation of esters, amides, and other derivatives with tailored properties.

One of the most promising applications of 2,7,8-TRIMETILQUINOLINE-3-CARBOXYLIC ACID lies in the pharmaceutical industry. Recent studies have explored its potential as a precursor for antimicrobial agents and anti-inflammatory compounds. The quinoline scaffold is a common motif in many FDA-approved drugs, and modifications to this structure can lead to enhanced bioactivity and selectivity. Researchers are particularly interested in its role in developing new treatments for infectious diseases, given the rising global concern over antibiotic resistance.

In addition to pharmaceuticals, 2,7,8-TRIMETILQUINOLINE-3-CARBOXYLIC ACID has found utility in the agrochemical sector. Its derivatives are being investigated for their potential as plant growth regulators and pesticides. The compound's ability to interact with biological systems makes it a candidate for developing eco-friendly agrochemicals that minimize environmental impact while maintaining efficacy. This aligns with the growing demand for sustainable agricultural solutions, a topic of significant interest among farmers and environmentalists alike.

The material science community has also taken note of 2,7,8-TRIMETILQUINOLINE-3-CARBOXYLIC ACID. Its aromatic structure and functional groups make it a potential candidate for designing advanced polymers and organic electronic materials. Researchers are exploring its use in organic light-emitting diodes (OLEDs) and photovoltaic cells, where its electron-rich quinoline core could enhance charge transport properties. This application is particularly relevant given the global push toward renewable energy and energy-efficient technologies.

Synthetic methodologies for 2,7,8-TRIMETILQUINOLINE-3-CARBOXYLIC ACID have evolved over the years, with recent advancements focusing on green chemistry approaches. Catalytic methods and solvent-free reactions are being developed to improve yield and reduce environmental impact. These innovations are critical as industries worldwide strive to adopt more sustainable practices, a trend that resonates with environmentally conscious consumers and regulatory bodies.

Market trends indicate a growing demand for 2,7,8-TRIMETILQUINOLINE-3-CARBOXYLIC ACID, driven by its diverse applications. The compound is increasingly available through specialized chemical suppliers, catering to the needs of research institutions and industrial laboratories. Its pricing and availability are influenced by factors such as raw material costs, synthesis complexity, and regional demand, making it essential for buyers to stay informed about market dynamics.

Quality control and analytical characterization are paramount when working with 2,7,8-TRIMETILQUINOLINE-3-CARBOXYLIC ACID. Techniques such as high-performance liquid chromatography (HPLC), nuclear magnetic resonance (NMR) spectroscopy, and mass spectrometry are commonly employed to ensure purity and confirm structural integrity. These analytical methods are crucial for researchers and manufacturers who rely on consistent and high-quality batches for their applications.

Looking ahead, the future of 2,7,8-TRIMETILQUINOLINE-3-CARBOXYLIC ACID appears bright, with ongoing research uncovering new potential uses. Its role in medicinal chemistry, sustainable agriculture, and advanced materials positions it as a compound of enduring relevance. As scientific understanding deepens and technological capabilities expand, this quinoline derivative is poised to play an increasingly important role in addressing some of the world's most pressing challenges.

For researchers and industry professionals seeking to explore the potential of 2,7,8-TRIMETILQUINOLINE-3-CARBOXYLIC ACID, staying abreast of the latest developments is essential. Collaborations between academia and industry, along with continued investment in R&D, will be key to unlocking the full spectrum of possibilities offered by this remarkable compound.

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