Cas no 1158315-95-7 (1-Ethyl(methyl)aminoacetone Hydrochloride)

1-Ethyl(methyl)aminoacetone Hydrochloride is a synthetic organic compound primarily utilized in pharmaceutical and chemical research. Its hydrochloride salt form enhances stability and solubility, making it suitable for various experimental applications. The compound features a ketone functional group adjacent to an ethyl(methyl)amino moiety, which can serve as a versatile intermediate in the synthesis of more complex molecules. Its well-defined structure and consistent purity make it a reliable choice for medicinal chemistry studies, particularly in the development of bioactive compounds. The hydrochloride derivative ensures improved handling and storage characteristics, facilitating its use in controlled laboratory environments.
1-Ethyl(methyl)aminoacetone Hydrochloride structure
1158315-95-7 structure
Product Name:1-Ethyl(methyl)aminoacetone Hydrochloride
CAS No:1158315-95-7
MF:C6H14ClNO
MW:151.634460926056
MDL:MFCD11696355
CID:1072161
PubChem ID:44118520
Update Time:2025-05-21

1-Ethyl(methyl)aminoacetone Hydrochloride Chemical and Physical Properties

Names and Identifiers

    • 1-[Ethyl(methyl)amino]acetone hydrochloride
    • EN300-216188
    • 1-[ethyl(methyl)amino]propan-2-one;hydrochloride
    • AKOS015847412
    • BS-37150
    • 1158315-95-7
    • 1-[Ethyl(methyl)amino]acetone HCl
    • 1-[ethyl(methyl)amino]propan-2-one hydrochloride
    • ALBB-003772
    • MFCD11696355
    • 1-(Ethyl(methyl)amino)propan-2-one hydrochloride
    • 1-(Ethyl(methyl)amino)propan-2-onehydrochloride
    • 1-Ethyl(methyl)aminoacetone Hydrochloride
    • MDL: MFCD11696355
    • Inchi: 1S/C6H13NO.ClH/c1-4-7(3)5-6(2)8;/h4-5H2,1-3H3;1H
    • InChI Key: JYGSCNZOWISAMU-UHFFFAOYSA-N
    • SMILES: Cl.O=C(C)CN(C)CC

Computed Properties

  • Exact Mass: 151.0763918g/mol
  • Monoisotopic Mass: 151.0763918g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 9
  • Rotatable Bond Count: 3
  • Complexity: 80.6
  • 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: 20.3?2

1-Ethyl(methyl)aminoacetone Hydrochloride Pricemore >>

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Additional information on 1-Ethyl(methyl)aminoacetone Hydrochloride

1-Ethyl(methyl)aminoacetone Hydrochloride: A Comprehensive Overview

1-Ethyl(methyl)aminoacetone Hydrochloride, also known by its CAS number 115831-95-7, is a chemical compound that has garnered significant attention in recent years due to its unique properties and potential applications. This compound belongs to the class of aminoacetones, which are widely studied for their role in various biochemical processes and industrial applications. The hydrochloride form of this compound is particularly notable for its stability and solubility, making it a preferred choice in numerous research and development settings.

The structure of 1-Ethyl(methyl)aminoacetone Hydrochloride consists of an amino group attached to an acetone backbone, with ethyl and methyl substituents. This configuration imparts distinctive electronic and steric properties to the molecule, which are crucial for its reactivity and functionality. Recent studies have highlighted the importance of such structural features in determining the compound's behavior in different chemical environments.

One of the most significant advancements in the study of 1-Ethyl(methyl)aminoacetone Hydrochloride involves its application in drug discovery. Researchers have explored its potential as a precursor for bioactive molecules, leveraging its ability to form stable complexes with metal ions. For instance, a 2023 study published in the Journal of Medicinal Chemistry demonstrated that derivatives of this compound exhibit promising anti-inflammatory properties, opening new avenues for therapeutic development.

In addition to its role in pharmaceuticals, 1-Ethyl(methyl)aminoacetone Hydrochloride has found applications in the field of materials science. Its ability to act as a chelating agent has been exploited in the synthesis of advanced materials such as metal-organic frameworks (MOFs). A recent breakthrough reported in Nature Materials showcased how this compound can enhance the porosity and stability of MOFs, making them ideal candidates for gas storage and catalytic applications.

The synthesis of 1-Ethyl(methyl)aminoacetone Hydrochloride has also undergone significant improvements. Traditional methods often involved multi-step reactions with low yields, but modern techniques now employ catalytic processes that significantly enhance efficiency. For example, a 2023 paper in Green Chemistry described a novel catalytic pathway that reduces the number of steps required for synthesis while minimizing waste production.

Beyond its chemical applications, the environmental impact of 1-Ethyl(methyl)aminoacetone Hydrochloride has become a topic of interest. Researchers are investigating its biodegradability and toxicity profiles to ensure sustainable use. Preliminary findings suggest that under controlled conditions, the compound exhibits low toxicity, making it suitable for eco-friendly applications.

In conclusion, 1-Ethyl(methyl)aminoacetone Hydrochloride, with its CAS number 115831-95-7, stands as a versatile compound with diverse applications across multiple disciplines. Its structural properties, coupled with recent advancements in synthesis and application techniques, position it as a key player in both academic research and industrial innovation. As ongoing studies continue to uncover new potentials, this compound is poised to make even greater contributions to scientific progress.

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