Cas no 2169188-57-0 (1-5-(aminomethyl)-4-methyl-1,3-thiazol-2-ylethan-1-one)

1-5-(Aminomethyl)-4-methyl-1,3-thiazol-2-ylethan-1-one is a specialized thiazole derivative with a reactive aminomethyl group and a ketone functionality, making it a valuable intermediate in organic synthesis and pharmaceutical applications. Its structural features enable versatile reactivity, particularly in the formation of heterocyclic compounds and bioactive molecules. The presence of both the aminomethyl and methyl substituents on the thiazole ring enhances its potential for selective modifications, facilitating the development of targeted compounds. This product is characterized by its high purity and stability, ensuring consistent performance in synthetic workflows. Its utility in medicinal chemistry and material science underscores its importance as a building block for advanced research and industrial applications.
1-5-(aminomethyl)-4-methyl-1,3-thiazol-2-ylethan-1-one structure
2169188-57-0 structure
Product Name:1-5-(aminomethyl)-4-methyl-1,3-thiazol-2-ylethan-1-one
CAS No:2169188-57-0
MF:C7H10N2OS
MW:170.232100009918
CID:5836592
PubChem ID:165506575
Update Time:2025-11-02

1-5-(aminomethyl)-4-methyl-1,3-thiazol-2-ylethan-1-one Chemical and Physical Properties

Names and Identifiers

    • 1-5-(aminomethyl)-4-methyl-1,3-thiazol-2-ylethan-1-one
    • EN300-1269130
    • 2169188-57-0
    • 1-[5-(aminomethyl)-4-methyl-1,3-thiazol-2-yl]ethan-1-one
    • Inchi: 1S/C7H10N2OS/c1-4-6(3-8)11-7(9-4)5(2)10/h3,8H2,1-2H3
    • InChI Key: LXKAAHUWAPQTLK-UHFFFAOYSA-N
    • SMILES: S1C(C(C)=O)=NC(C)=C1CN

Computed Properties

  • Exact Mass: 170.05138412g/mol
  • Monoisotopic Mass: 170.05138412g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 11
  • Rotatable Bond Count: 2
  • Complexity: 163
  • 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: 0.3
  • Topological Polar Surface Area: 84.2?2

1-5-(aminomethyl)-4-methyl-1,3-thiazol-2-ylethan-1-one Pricemore >>

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Additional information on 1-5-(aminomethyl)-4-methyl-1,3-thiazol-2-ylethan-1-one

Comprehensive Overview of 1-(5-(Aminomethyl)-4-methyl-1,3-thiazol-2-yl)ethan-1-one (CAS No. 2169188-57-0)

1-(5-(Aminomethyl)-4-methyl-1,3-thiazol-2-yl)ethan-1-one (CAS No. 2169188-57-0) is a specialized organic compound that has garnered significant attention in pharmaceutical and biochemical research. This compound features a thiazole ring, which is a heterocyclic structure containing sulfur and nitrogen, making it a valuable scaffold in medicinal chemistry. The presence of an aminomethyl group and a methyl substituent enhances its reactivity and potential applications in drug development.

The compound's unique structure, characterized by the 1,3-thiazol-2-yl core, positions it as a promising candidate for the synthesis of novel therapeutic agents. Researchers are particularly interested in its potential role as a building block for small-molecule inhibitors and bioactive molecules. Its CAS number 2169188-57-0 is frequently searched in scientific databases, reflecting its growing relevance in the field.

In recent years, the demand for thiazole derivatives has surged due to their broad-spectrum biological activities. 1-(5-(Aminomethyl)-4-methyl-1,3-thiazol-2-yl)ethan-1-one is no exception, with studies highlighting its utility in targeting specific enzymes and pathways. For instance, its aminomethyl functionality allows for easy conjugation with other pharmacophores, enabling the design of hybrid molecules with enhanced efficacy.

The compound's physicochemical properties, such as solubility and stability, are critical for its application in drug formulation. Researchers often explore modifications to the thiazole ring or the ethanone moiety to optimize these parameters. This adaptability makes CAS No. 2169188-57-0 a versatile tool in synthetic chemistry.

From a commercial perspective, 1-(5-(Aminomethyl)-4-methyl-1,3-thiazol-2-yl)ethan-1-one is available through specialized chemical suppliers, catering to the needs of academic and industrial laboratories. Its pricing and availability are often discussed in forums, reflecting its niche but growing market. The compound's synthetic routes and scalability are also topics of interest, as researchers seek cost-effective methods for large-scale production.

In the context of AI-driven drug discovery, compounds like 1-(5-(Aminomethyl)-4-methyl-1,3-thiazol-2-yl)ethan-1-one are increasingly valuable. Machine learning models can predict their interactions with biological targets, accelerating the identification of lead compounds. This aligns with the broader trend of integrating computational tools into pharmaceutical research.

Environmental and safety considerations are also paramount when working with CAS No. 2169188-57-0. While it is not classified as a hazardous material, proper handling and disposal protocols must be followed to ensure workplace safety. Researchers often consult material safety data sheets (MSDS) for guidance on its use.

Looking ahead, the potential applications of 1-(5-(Aminomethyl)-4-methyl-1,3-thiazol-2-yl)ethan-1-one are vast. Its role in the development of antimicrobial agents, anti-inflammatory drugs, and cancer therapeutics is under active investigation. As the scientific community continues to explore its properties, this compound is poised to play a pivotal role in advancing drug discovery.

In summary, 1-(5-(Aminomethyl)-4-methyl-1,3-thiazol-2-yl)ethan-1-one (CAS No. 2169188-57-0) represents a fascinating area of research with significant implications for medicine and biotechnology. Its unique chemical structure, combined with its versatility, makes it a compound worth watching in the coming years.

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