Cas no 97454-46-1 (N-ethyl-2-(ethylamino)acetamide)

N-Ethyl-2-(ethylamino)acetamide is a versatile organic compound characterized by its amide and amine functional groups, making it useful in synthetic chemistry and pharmaceutical applications. Its structure allows for reactivity in nucleophilic substitution and condensation reactions, serving as an intermediate in the synthesis of more complex molecules. The compound exhibits moderate solubility in polar solvents, facilitating its use in solution-phase reactions. Its stability under standard conditions and well-defined reactivity profile make it a reliable choice for researchers developing bioactive compounds or specialty chemicals. The presence of ethyl substituents enhances its lipophilicity, which can be advantageous in drug design or agrochemical formulations.
N-ethyl-2-(ethylamino)acetamide structure
97454-46-1 structure
Product Name:N-ethyl-2-(ethylamino)acetamide
CAS No:97454-46-1
MF:C6H14N2O
MW:130.188161373138
CID:812780
PubChem ID:2466702
Update Time:2025-10-29

N-ethyl-2-(ethylamino)acetamide Chemical and Physical Properties

Names and Identifiers

    • Acetamide,N-ethyl-2-(ethylamino)-
    • N-ethyl-2-(ethylamino)acetamide
    • AKOS000200926
    • Z55849446
    • SCHEMBL1790228
    • CS-0224659
    • MFCD06380313
    • DTXSID30368761
    • 97454-46-1
    • EN300-12036
    • QXEXBEVZURKZKK-UHFFFAOYSA-N
    • MDL: MFCD06380313
    • Inchi: 1S/C6H14N2O/c1-3-7-5-6(9)8-4-2/h7H,3-5H2,1-2H3,(H,8,9)
    • InChI Key: QXEXBEVZURKZKK-UHFFFAOYSA-N
    • SMILES: O=C(CNCC)NCC

Computed Properties

  • Exact Mass: 131.118438
  • Monoisotopic Mass: 131.118438
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 9
  • Rotatable Bond Count: 5
  • Complexity: 83.1
  • 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
  • Topological Polar Surface Area: 45.7
  • XLogP3: -0.1

Experimental Properties

  • Boiling Point: 256.2°Cat760mmHg
  • Flash Point: 115.6°C

N-ethyl-2-(ethylamino)acetamide Pricemore >>

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Additional information on N-ethyl-2-(ethylamino)acetamide

N-Ethyl-2-(Ethylamino)Acetamide: A Comprehensive Overview

N-Ethyl-2-(Ethylamino)Acetamide, also known by its CAS number 97454-46-1, is a compound of significant interest in various fields of chemistry and pharmacology. This compound has been studied extensively for its potential applications in drug development, agricultural chemicals, and industrial processes. The structure of N-Ethyl-2-(Ethylamino)Acetamide consists of an acetamide group with ethyl substituents, which contributes to its unique chemical properties and reactivity.

Recent studies have highlighted the importance of N-Ethyl-2-(Ethylamino)Acetamide in the development of novel therapeutic agents. Researchers have explored its role as a building block for creating bioactive molecules, particularly in the design of peptide analogs and inhibitors for various enzymes. The compound's ability to form stable amide bonds makes it a valuable intermediate in organic synthesis.

One of the key areas of research involving N-Ethyl-2-(Ethylamino)Acetamide is its application in medicinal chemistry. Scientists have investigated its potential as a precursor for developing drugs targeting neurodegenerative diseases, cancer, and infectious agents. For instance, studies have shown that derivatives of this compound can modulate the activity of certain kinases, which are critical in cellular signaling pathways.

In addition to its medicinal applications, N-Ethyl-2-(Ethylamino)Acetamide has also been examined for its role in agrochemicals. Researchers have explored its potential as a plant growth regulator or as an ingredient in pesticides. The compound's ability to interact with biological systems at the molecular level makes it a promising candidate for developing environmentally friendly agricultural solutions.

The synthesis of N-Ethyl-2-(Ethylamino)Acetamide involves several steps, including nucleophilic acylation and alkylation reactions. Recent advancements in catalytic methods have improved the efficiency and selectivity of these reactions, enabling the large-scale production of this compound. Moreover, green chemistry approaches have been adopted to minimize waste and reduce the environmental impact of its manufacturing process.

From a structural perspective, N-Ethyl-2-(Ethylamino)Acetamide exhibits interesting physical properties, such as solubility in organic solvents and moderate stability under physiological conditions. These characteristics make it suitable for use in various experimental setups, including cell culture assays and animal models.

Looking ahead, the continued exploration of N-Ethyl-2-(Ethylamino)Acetamide's properties is expected to yield new insights into its potential applications. Collaborative efforts between academic institutions and industry partners are likely to accelerate the development of innovative products based on this compound.

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