Cas no 57369-93-4 (2-hydrazinyl-4,8-dimethylquinoline)

2-Hydrazinyl-4,8-dimethylquinoline is a specialized quinoline derivative featuring a hydrazinyl functional group at the 2-position and methyl substituents at the 4- and 8-positions. This compound is of interest in organic synthesis and pharmaceutical research due to its potential as a versatile building block for heterocyclic chemistry. The hydrazinyl moiety enables condensation reactions, facilitating the formation of hydrazones and other nitrogen-containing heterocycles, while the dimethylquinoline core contributes to stability and lipophilicity. Its structural features make it suitable for applications in medicinal chemistry, particularly in the development of bioactive molecules. The compound is typically handled under controlled conditions due to its reactive functional groups.
2-hydrazinyl-4,8-dimethylquinoline structure
57369-93-4 structure
Product Name:2-hydrazinyl-4,8-dimethylquinoline
CAS No:57369-93-4
MF:C11H13N3
MW:187.241021871567
CID:382967
PubChem ID:3684316
Update Time:2025-11-05

2-hydrazinyl-4,8-dimethylquinoline Chemical and Physical Properties

Names and Identifiers

    • Quinoline,2-hydrazinyl-4,8-dimethyl-
    • (4,8-dimethylquinolin-2-yl)hydrazine
    • 2-HYDRAZINO-4,8-DIMETHYLQUINOLINE
    • 2-hydrazinyl-4,8-dimethylQuinoline
    • 2-hydrazino-4,8-dimethyl-quinoline
    • 4,8-dimethyl-2-quinolyhydrazine
    • 4,8-dimethyl-2-quinolylhydrazine
    • AC1MVJOV
    • AC1Q2J5C
    • CTK5A6747
    • SureCN1577707
    • DTXSID70395011
    • SB67859
    • FT-0736250
    • 57369-93-4
    • SCHEMBL1577707
    • F3284-7646
    • EN300-09211
    • IDGTZROMJOZLQC-UHFFFAOYSA-N
    • Z55993087
    • AKOS002359932
    • 2-hydrazinyl-4,8-dimethylquinoline
    • MDL： MFCD02197923
    • Inchi： 1S/C11H13N3/c1-7-4-3-5-9-8(2)6-10(14-12)13-11(7)9/h3-6H,12H2,1-2H3,(H,13,14)
    • InChI Key： IDGTZROMJOZLQC-UHFFFAOYSA-N
    • SMILES： N1C(=CC(C)=C2C=CC=C(C)C=12)NN

Computed Properties

  • Exact Mass: 187.11109
  • Monoisotopic Mass: 187.110947427g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 1
  • Complexity: 195
  • 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: 2.5
  • Topological Polar Surface Area: 50.9?2

Experimental Properties

  • PSA: 50.94

2-hydrazinyl-4,8-dimethylquinoline Pricemore >>

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2-hydrazinyl-4,8-dimethylquinoline Related Literature

Additional information on 2-hydrazinyl-4,8-dimethylquinoline

Comprehensive Overview of 2-Hydrazinyl-4,8-dimethylquinoline (CAS No. 57369-93-4): Properties, Applications, and Innovations

2-Hydrazinyl-4,8-dimethylquinoline (CAS No. 57369-93-4) is a specialized quinoline derivative with a unique molecular structure that combines a hydrazine functional group with a dimethyl-substituted quinoline core. This compound has garnered significant attention in pharmaceutical and agrochemical research due to its potential as a building block for synthesizing biologically active molecules. Its CAS number 57369-93-4 serves as a critical identifier in chemical databases, ensuring precise tracking in industrial and academic settings.

In recent years, the demand for heterocyclic compounds like 2-hydrazinyl-4,8-dimethylquinoline has surged, driven by advancements in drug discovery and material science. Researchers are particularly interested in its role as a precursor for antimicrobial agents and anticancer drugs, aligning with global health priorities. The compound’s structural versatility allows modifications to enhance bioavailability and target specificity, making it a focal point in medicinal chemistry.

From a synthetic chemistry perspective, CAS 57369-93-4 exhibits notable reactivity due to its hydrazinyl group, which facilitates condensation reactions and cyclization processes. This property is leveraged in designing fluorescent probes and coordination complexes, addressing trends in bioimaging and catalysis. Users searching for "quinoline-based hydrazine derivatives" or "applications of 2-hydrazinyl-4,8-dimethylquinoline" often seek insights into these cutting-edge applications.

Environmental and green chemistry considerations are also shaping the discourse around 57369-93-4. Innovations in solvent-free synthesis and catalytic efficiency aim to reduce the ecological footprint of producing such compounds. Queries like "sustainable synthesis of quinoline derivatives" reflect growing user interest in eco-friendly methodologies, positioning 2-hydrazinyl-4,8-dimethylquinoline as a case study for green innovation.

Analytical characterization of 2-hydrazinyl-4,8-dimethylquinoline relies on techniques like NMR spectroscopy, mass spectrometry, and HPLC, ensuring purity and consistency for industrial use. The compound’s stability under ambient conditions and solubility profiles are frequently discussed in forums, highlighting practical handling considerations.

Looking ahead, the integration of AI-driven molecular modeling is accelerating the exploration of 57369-93-4 derivatives. Searches for "computational chemistry in quinoline research" underscore the intersection of technology and traditional synthesis. As patents and publications citing CAS No. 57369-93-4 multiply, this compound remains a keystone in advancing functional materials and therapeutic agents.

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