Cas no 223128-18-5 (ethyl 2-(ethylamino)propanoate)

Ethyl 2-(ethylamino)propanoate is an ester derivative with a secondary amine functional group, characterized by its versatile reactivity and solubility in organic solvents. Its molecular structure, combining an ethyl ester and an ethylamino moiety, makes it a valuable intermediate in organic synthesis, particularly for the preparation of pharmaceuticals, agrochemicals, and specialty chemicals. The compound exhibits favorable stability under standard conditions and can participate in reactions such as amidation, alkylation, and condensation. Its balanced lipophilicity enhances its utility in formulations requiring controlled solubility profiles. Ethyl 2-(ethylamino)propanoate is often employed in research and industrial applications where tailored amine-ester functionalities are required.
ethyl 2-(ethylamino)propanoate structure
223128-18-5 structure
Product Name:ethyl 2-(ethylamino)propanoate
CAS No:223128-18-5
MF:C7H15NO2
MW:145.199502229691
MDL:MFCD12150745
CID:244486
PubChem ID:19002560
Update Time:2025-11-02

ethyl 2-(ethylamino)propanoate Chemical and Physical Properties

Names and Identifiers

    • Alanine, N-ethyl-,ethyl ester
    • Alanine, N-ethyl-, ethyl ester (9CI)
    • ethyl 2-(ethylamino)propanoate
    • 223128-18-5
    • SCHEMBL3598471
    • L-Alanine, N-ethyl-, ethyl ester (9CI)
    • EN300-863788
    • 149912-14-1
    • MDL: MFCD12150745
    • Inchi: 1S/C7H15NO2/c1-4-8-6(3)7(9)10-5-2/h6,8H,4-5H2,1-3H3
    • InChI Key: VKPHXAZSBHQZRC-UHFFFAOYSA-N
    • SMILES: O(CC)C(C(C)NCC)=O

Computed Properties

  • Exact Mass: 145.110278721g/mol
  • Monoisotopic Mass: 145.110278721g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 5
  • Complexity: 104
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 1
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 0.9
  • Topological Polar Surface Area: 38.3?2

ethyl 2-(ethylamino)propanoate Pricemore >>

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Additional information on ethyl 2-(ethylamino)propanoate

Recent Advances in the Study of Ethyl 2-(Ethylamino)Propanoate (CAS 223128-18-5) in Chemical Biology and Pharmaceutical Research

Ethyl 2-(ethylamino)propanoate (CAS 223128-18-5) is a compound of growing interest in the field of chemical biology and pharmaceutical research. Recent studies have highlighted its potential as a versatile intermediate in the synthesis of bioactive molecules and its role in modulating biological pathways. This research brief aims to provide an overview of the latest findings related to this compound, focusing on its chemical properties, synthetic applications, and pharmacological potential.

One of the key areas of investigation has been the synthesis and optimization of ethyl 2-(ethylamino)propanoate. Researchers have developed novel synthetic routes to improve the yield and purity of this compound, which is critical for its application in drug discovery. For instance, a recent study published in the Journal of Medicinal Chemistry demonstrated an efficient one-pot synthesis method that significantly reduces the production cost and environmental impact. This advancement is particularly relevant for large-scale pharmaceutical manufacturing.

In addition to its synthetic utility, ethyl 2-(ethylamino)propanoate has shown promise as a precursor for the development of new therapeutic agents. A 2023 study in Bioorganic & Medicinal Chemistry Letters reported that derivatives of this compound exhibit notable activity against certain enzyme targets involved in inflammatory diseases. The study utilized molecular docking and in vitro assays to validate the compound's binding affinity and inhibitory effects, suggesting its potential as a lead compound for further drug development.

Another significant finding comes from a recent preprint on bioRxiv, where researchers explored the pharmacokinetic properties of ethyl 2-(ethylamino)propanoate in animal models. The study revealed favorable absorption and distribution profiles, along with a relatively low toxicity profile, making it a candidate for further preclinical evaluation. These findings are particularly encouraging for the development of orally administered drugs.

Despite these promising results, challenges remain in the clinical translation of ethyl 2-(ethylamino)propanoate-based therapeutics. A review article in Current Opinion in Chemical Biology highlighted the need for more comprehensive toxicity studies and formulation optimization to address potential stability issues. Future research directions may include the exploration of prodrug strategies and the development of targeted delivery systems to enhance the compound's efficacy and safety.

In conclusion, ethyl 2-(ethylamino)propanoate (CAS 223128-18-5) represents a valuable scaffold in chemical biology and pharmaceutical research. Its synthetic versatility, biological activity, and favorable pharmacokinetic properties underscore its potential for therapeutic applications. Continued research efforts will be essential to fully realize its clinical potential and address existing challenges.

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