Cas no 2694744-99-3 (1-(2,4-Dichloro-1,3-thiazol-5-yl)methanamine hydrochloride)

1-(2,4-Dichloro-1,3-thiazol-5-yl)methanamine hydrochloride is a specialized organic compound featuring a dichlorothiazole core with an aminomethyl functional group. Its structural properties make it a valuable intermediate in pharmaceutical and agrochemical synthesis, particularly in the development of biologically active molecules. The hydrochloride salt enhances stability and solubility, facilitating handling and reactivity in synthetic processes. The presence of chlorine atoms on the thiazole ring contributes to its potential as a precursor for further functionalization, enabling diverse derivatization pathways. This compound is suited for applications requiring precise molecular modifications, offering a balance of reactivity and selectivity for advanced chemical synthesis.
1-(2,4-Dichloro-1,3-thiazol-5-yl)methanamine hydrochloride structure
2694744-99-3 structure
Product Name:1-(2,4-Dichloro-1,3-thiazol-5-yl)methanamine hydrochloride
CAS No:2694744-99-3
MF:C4H5Cl3N2S
MW:219.519896268845
MDL:MFCD34475595
CID:5627804
PubChem ID:165951435
Update Time:2025-05-27

1-(2,4-Dichloro-1,3-thiazol-5-yl)methanamine hydrochloride Chemical and Physical Properties

Names and Identifiers

    • 2694744-99-3
    • 1-(2,4-dichloro-1,3-thiazol-5-yl)methanamine hydrochloride
    • EN300-28338075
    • 1-(2,4-Dichloro-1,3-thiazol-5-yl)methanamine hydrochloride
    • MDL: MFCD34475595
    • Inchi: 1S/C4H4Cl2N2S.ClH/c5-3-2(1-7)9-4(6)8-3;/h1,7H2;1H
    • InChI Key: FTJWKZAUZNBWCA-UHFFFAOYSA-N
    • SMILES: ClC1=C(CN)SC(=N1)Cl.Cl

Computed Properties

  • Exact Mass: 217.923902g/mol
  • Monoisotopic Mass: 217.923902g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 1
  • Complexity: 103
  • Covalently-Bonded Unit Count: 2
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • Topological Polar Surface Area: 67.2?2

1-(2,4-Dichloro-1,3-thiazol-5-yl)methanamine hydrochloride Pricemore >>

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Additional information on 1-(2,4-Dichloro-1,3-thiazol-5-yl)methanamine hydrochloride

Recent Advances in the Study of 1-(2,4-Dichloro-1,3-thiazol-5-yl)methanamine Hydrochloride (CAS: 2694744-99-3)

1-(2,4-Dichloro-1,3-thiazol-5-yl)methanamine hydrochloride (CAS: 2694744-99-3) is a chemical compound of significant interest in the field of chemical biology and pharmaceutical research. Recent studies have explored its potential applications in drug discovery, particularly as a building block for the synthesis of novel therapeutic agents. This research brief aims to summarize the latest findings related to this compound, focusing on its chemical properties, biological activities, and potential therapeutic applications.

Recent literature highlights the role of 1-(2,4-Dichloro-1,3-thiazol-5-yl)methanamine hydrochloride in the development of small-molecule inhibitors targeting various enzymes and receptors. Its unique structural features, including the dichlorothiazole moiety, make it a valuable scaffold for medicinal chemistry. Studies have demonstrated its utility in the synthesis of compounds with antimicrobial, antiviral, and anticancer properties. For instance, derivatives of this compound have shown promising activity against resistant bacterial strains and certain types of cancer cells.

One of the key advancements in the study of this compound is its application in the design of kinase inhibitors. Kinases are critical targets in the treatment of various diseases, including cancer and inflammatory disorders. Researchers have successfully incorporated 1-(2,4-Dichloro-1,3-thiazol-5-yl)methanamine hydrochloride into kinase inhibitor scaffolds, resulting in compounds with enhanced selectivity and potency. These findings underscore the compound's potential as a versatile tool in drug discovery.

In addition to its role in kinase inhibition, recent studies have explored the compound's interactions with other biological targets. For example, it has been investigated as a modulator of G-protein-coupled receptors (GPCRs), which are involved in a wide range of physiological processes. Preliminary results suggest that derivatives of this compound may exhibit selective binding to specific GPCR subtypes, opening new avenues for the development of targeted therapies.

The synthesis and characterization of 1-(2,4-Dichloro-1,3-thiazol-5-yl)methanamine hydrochloride have also been refined in recent years. Improved synthetic routes have been developed to enhance yield and purity, facilitating its use in large-scale pharmaceutical production. Analytical techniques such as NMR spectroscopy and mass spectrometry have been employed to confirm the compound's structure and purity, ensuring its suitability for further research and development.

Despite these advancements, challenges remain in the optimization of this compound for clinical use. Issues such as bioavailability, metabolic stability, and toxicity need to be addressed through further structural modifications and preclinical studies. However, the progress made thus far highlights the compound's potential as a cornerstone in the development of next-generation therapeutics.

In conclusion, 1-(2,4-Dichloro-1,3-thiazol-5-yl)methanamine hydrochloride (CAS: 2694744-99-3) represents a promising candidate for drug discovery, with applications spanning multiple therapeutic areas. Ongoing research is expected to uncover new opportunities for its use, paving the way for innovative treatments for various diseases. This brief provides a snapshot of the current state of research, emphasizing the compound's versatility and potential impact on the pharmaceutical industry.

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