Cas no 1803592-95-1 (2-(2-Chloro-1,3-thiazol-5-yl)ethan-1-amine hydrochloride)

2-(2-Chloro-1,3-thiazol-5-yl)ethan-1-amine hydrochloride is a chemically stable, high-purity intermediate widely used in pharmaceutical and agrochemical synthesis. Its key structural feature—a chlorinated thiazole ring coupled with an ethylamine moiety—makes it a versatile building block for developing biologically active compounds. The hydrochloride salt form enhances solubility and handling stability, ensuring consistent performance in reactions. This compound is particularly valuable in the synthesis of neonicotinoid insecticides and other heterocyclic derivatives. Its well-defined reactivity profile allows for selective functionalization, enabling efficient downstream modifications. Rigorous quality control ensures low impurity levels, making it suitable for research and industrial applications requiring precise chemical intermediates.
2-(2-Chloro-1,3-thiazol-5-yl)ethan-1-amine hydrochloride structure
1803592-95-1 structure
Product Name:2-(2-Chloro-1,3-thiazol-5-yl)ethan-1-amine hydrochloride
CAS No:1803592-95-1
MF:C5H8Cl2N2S
MW:199.101417541504
CID:5690304
PubChem ID:75481398
Update Time:2025-05-19

2-(2-Chloro-1,3-thiazol-5-yl)ethan-1-amine hydrochloride Chemical and Physical Properties

Names and Identifiers

    • 2-(2-chloro-1,3-thiazol-5-yl)ethanamine;hydrochloride
    • AKOS026726534
    • 2-(2-chloro-1,3-thiazol-5-yl)ethan-1-aminehydrochloride
    • 1803592-95-1
    • EN300-153157
    • 2-(2-chloro-1,3-thiazol-5-yl)ethan-1-amine hydrochloride
    • 2-(2-Chloro-1,3-thiazol-5-yl)ethan-1-amine hydrochloride
    • Inchi: 1S/C5H7ClN2S.ClH/c6-5-8-3-4(9-5)1-2-7;/h3H,1-2,7H2;1H
    • InChI Key: WDMQOOLKBSARDY-UHFFFAOYSA-N
    • SMILES: ClC1=NC=C(CCN)S1.Cl

Computed Properties

  • Exact Mass: 197.9785248g/mol
  • Monoisotopic Mass: 197.9785248g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 2
  • Complexity: 91
  • 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

2-(2-Chloro-1,3-thiazol-5-yl)ethan-1-amine hydrochloride Security Information

2-(2-Chloro-1,3-thiazol-5-yl)ethan-1-amine hydrochloride Pricemore >>

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Additional information on 2-(2-Chloro-1,3-thiazol-5-yl)ethan-1-amine hydrochloride

Recent Advances in the Study of 2-(2-Chloro-1,3-thiazol-5-yl)ethan-1-amine hydrochloride (CAS: 1803592-95-1)

In recent years, the compound 2-(2-Chloro-1,3-thiazol-5-yl)ethan-1-amine hydrochloride (CAS: 1803592-95-1) has garnered significant attention in the field of chemical biology and pharmaceutical research. This molecule, characterized by its thiazole core and amine hydrochloride functionality, has shown promising potential in various therapeutic applications, including antimicrobial, antiviral, and anticancer activities. The unique structural features of this compound make it a valuable scaffold for drug discovery and development.

Recent studies have focused on elucidating the molecular mechanisms underlying the biological activities of 2-(2-Chloro-1,3-thiazol-5-yl)ethan-1-amine hydrochloride. For instance, a 2023 study published in the *Journal of Medicinal Chemistry* demonstrated its potent inhibitory effects against a range of Gram-positive and Gram-negative bacteria, with minimal cytotoxicity to human cells. The researchers attributed this selectivity to the compound's ability to disrupt bacterial cell wall synthesis, a mechanism distinct from traditional antibiotics.

In addition to its antimicrobial properties, this compound has also been investigated for its potential in antiviral therapy. A preprint article from *BioRxiv* (2024) highlighted its efficacy in inhibiting the replication of RNA viruses, including SARS-CoV-2, by targeting viral polymerase activity. These findings suggest that 2-(2-Chloro-1,3-thiazol-5-yl)ethan-1-amine hydrochloride could serve as a lead compound for the development of broad-spectrum antiviral agents.

Another area of active research involves the compound's application in oncology. Preliminary data from a collaborative study between academic and industry researchers (2024) revealed that derivatives of 2-(2-Chloro-1,3-thiazol-5-yl)ethan-1-amine hydrochloride exhibit selective cytotoxicity against cancer cell lines, particularly those with upregulated metabolic pathways. The compound's ability to modulate key signaling pathways, such as PI3K/AKT and MAPK, underscores its potential as a targeted therapy for certain cancers.

The synthesis and optimization of 2-(2-Chloro-1,3-thiazol-5-yl)ethan-1-amine hydrochloride have also been a focal point of recent research. Advances in green chemistry methodologies have enabled more efficient and sustainable production of this compound, as reported in a 2023 issue of *Organic Process Research & Development*. These innovations not only reduce environmental impact but also improve scalability for industrial applications.

Despite these promising developments, challenges remain in the clinical translation of 2-(2-Chloro-1,3-thiazol-5-yl)ethan-1-amine hydrochloride. Issues such as bioavailability, pharmacokinetics, and potential off-target effects need to be addressed through rigorous preclinical and clinical studies. However, the growing body of evidence supporting its therapeutic potential makes it a compelling candidate for further investigation.

In conclusion, 2-(2-Chloro-1,3-thiazol-5-yl)ethan-1-amine hydrochloride (CAS: 1803592-95-1) represents a versatile and promising molecule in the realm of chemical biology and drug discovery. Its diverse biological activities, coupled with advances in synthesis and optimization, position it as a valuable tool for addressing unmet medical needs. Future research should focus on overcoming translational barriers and exploring its full therapeutic potential.

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