Cas no 118134-24-0 (1-2-(dimethylamino)-1,3-thiazol-5-ylethan-1-one)

1-2-(Dimethylamino)-1,3-thiazol-5-ylethan-1-one is a specialized organic compound featuring a thiazole core substituted with a dimethylamino group and an acetyl moiety. This structure imparts unique reactivity, making it valuable as an intermediate in pharmaceutical and agrochemical synthesis. Its electron-rich thiazole ring enhances its utility in heterocyclic chemistry, particularly in the development of bioactive molecules. The compound's well-defined molecular architecture allows for precise functionalization, enabling tailored modifications for target applications. High purity and stability under standard conditions ensure consistent performance in synthetic workflows. Its compatibility with a range of reaction conditions further underscores its versatility in organic synthesis.
1-2-(dimethylamino)-1,3-thiazol-5-ylethan-1-one structure
118134-24-0 structure
Product Name:1-2-(dimethylamino)-1,3-thiazol-5-ylethan-1-one
CAS No:118134-24-0
MF:C7H10N2OS
MW:170.232100009918
CID:1210870
PubChem ID:822439
Update Time:2025-10-28

1-2-(dimethylamino)-1,3-thiazol-5-ylethan-1-one Chemical and Physical Properties

Names and Identifiers

    • Ethanone, 1-[2-(dimethylamino)-5-thiazolyl]-
    • 1-[2-(dimethylamino)-5-thiazolyl]Ethanone
    • 1-2-(dimethylamino)-1,3-thiazol-5-ylethan-1-one
    • SMR000113802
    • CS-0452797
    • AB-601/30963016
    • AKOS012050837
    • 1-(2-(Dimethylamino)thiazol-5-yl)ethan-1-one
    • CHEMBL1519985
    • DA-29994
    • 1-[2-(dimethylamino)-1,3-thiazol-5-yl]ethanone
    • EN300-1868978
    • 1-[2-(dimethylamino)-1,3-thiazol-5-yl]ethan-1-one
    • 118134-24-0
    • MLS000594522
    • 1-(2-(Dimethylamino)thiazol-5-yl)ethanone
    • HMS2314M17
    • Inchi: 1S/C7H10N2OS/c1-5(10)6-4-8-7(11-6)9(2)3/h4H,1-3H3
    • InChI Key: UCABLVINQYWAPR-UHFFFAOYSA-N
    • SMILES: S1C(C(C)=O)=CN=C1N(C)C

Computed Properties

  • Exact Mass: 170.0515
  • Monoisotopic Mass: 170.05138412g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 2
  • Complexity: 161
  • 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: 1.4
  • Topological Polar Surface Area: 61.4?2

Experimental Properties

  • PSA: 33.2

1-2-(dimethylamino)-1,3-thiazol-5-ylethan-1-one Pricemore >>

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1-2-(dimethylamino)-1,3-thiazol-5-ylethan-1-one Related Literature

Additional information on 1-2-(dimethylamino)-1,3-thiazol-5-ylethan-1-one

1-2-(Dimethylamino)-1,3-thiazol-5-ylethan-1-one: A Comprehensive Overview

The compound 1-2-(dimethylamino)-1,3-thiazol-5-ylethan-1-one, also known by its CAS number 118134-24-0, is a fascinating molecule with significant potential in various scientific and industrial applications. This compound belongs to the class of thiazoles, which are heterocyclic aromatic compounds with a five-membered ring containing sulfur and nitrogen atoms. The presence of the dimethylamino group and the ketone functionality in its structure makes it particularly interesting for researchers and industry professionals alike.

Recent studies have highlighted the importance of thiazole derivatives in drug discovery and development. The unique electronic properties of the thiazole ring, combined with the substituents on the molecule, can lead to diverse biological activities. For instance, dimethylamino groups are known to enhance lipophilicity and improve drug absorption, making this compound a promising candidate for pharmacological applications.

In terms of synthesis, 1-2-(dimethylamino)-1,3-thiazol-5-ylethan-1-one can be prepared through various routes, including condensation reactions involving thiols and aldehydes or ketones. The choice of synthetic method depends on the availability of starting materials and the desired purity of the final product. Researchers have also explored green chemistry approaches to synthesize this compound, which aligns with current trends toward sustainable chemical practices.

The physical properties of this compound are equally noteworthy. Its molecular weight is approximately 207.3 g/mol, and it has a melting point of around 95°C. The compound is soluble in common organic solvents such as dichloromethane and ethyl acetate, making it suitable for various laboratory applications. Its UV-vis spectrum shows strong absorption in the visible region, which could be exploited in photonic applications.

One of the most exciting aspects of this compound is its potential in pharmaceutical research. Several studies have demonstrated that thiazole derivatives exhibit anti-inflammatory, antioxidant, and anticancer activities. For example, a recent study published in the Journal of Medicinal Chemistry reported that derivatives of this compound showed significant inhibition against certain cancer cell lines. These findings suggest that further research into its biological activities could lead to novel therapeutic agents.

Beyond pharmacology, 1-2-(dimethylamino)-1,3-thiazol-5-ylethan-1-one has also found applications in materials science. Its ability to form stable coordination complexes with metal ions makes it a valuable ligand in catalysis and sensor development. Researchers have explored its use in creating metalloporphyrins for gas sensing applications, where its selectivity and sensitivity are highly advantageous.

In conclusion, 1-2-(dimethylamino)-1,3-thiazol-5-ylethan-1-one, with its unique chemical structure and versatile properties, continues to be a subject of intense research interest. As new studies emerge highlighting its potential applications in drug discovery, materials science, and beyond, this compound is poised to play a significant role in advancing scientific innovation.

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