Cas no 124186-08-9 (2-(Chloromethoxy)acetic Acid Ethyl Ester)

2-(Chloromethoxy)acetic Acid Ethyl Ester structure
124186-08-9 structure
Product Name:2-(Chloromethoxy)acetic Acid Ethyl Ester
CAS No:124186-08-9
MF:C5H9ClO3
MW:152.576161146164
CID:1063848
PubChem ID:11693932
Update Time:2025-07-19

2-(Chloromethoxy)acetic Acid Ethyl Ester Chemical and Physical Properties

Names and Identifiers

    • 2-(Chloromethoxy)acetic Acid Ethyl Ester
    • Ethyl2-(chloromethoxy)acetate
    • DB-312825
    • AKOS006382919
    • Ethyl 2-(chloromethoxy)acetate
    • Ethyl 2-(Chloromethoxy)acetate;
    • SCHEMBL1606254
    • 124186-08-9
    • Inchi: 1S/C5H9ClO3/c1-2-9-5(7)3-8-4-6/h2-4H2,1H3
    • InChI Key: GSWWPLIBOXOWMF-UHFFFAOYSA-N
    • SMILES: ClCOCC(=O)OCC

Computed Properties

  • Exact Mass: 152.0240218g/mol
  • Monoisotopic Mass: 152.0240218g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 9
  • Rotatable Bond Count: 5
  • Complexity: 84.3
  • 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: 1.1
  • Topological Polar Surface Area: 35.5?2

2-(Chloromethoxy)acetic Acid Ethyl Ester Pricemore >>

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Additional information on 2-(Chloromethoxy)acetic Acid Ethyl Ester

Research Briefing on 2-(Chloromethoxy)acetic Acid Ethyl Ester (CAS: 124186-08-9) in Chemical and Biomedical Applications

2-(Chloromethoxy)acetic Acid Ethyl Ester (CAS: 124186-08-9) is a chemical compound of significant interest in the fields of organic synthesis and pharmaceutical research. Recent studies have highlighted its utility as a versatile intermediate in the synthesis of more complex molecules, particularly in the development of novel therapeutic agents. This briefing provides an overview of the latest research findings, focusing on its chemical properties, synthetic applications, and potential biomedical implications.

In a 2023 study published in the Journal of Medicinal Chemistry, researchers explored the use of 2-(Chloromethoxy)acetic Acid Ethyl Ester as a key building block in the synthesis of antiviral compounds. The study demonstrated that the compound's reactive chloromethoxy and ester functional groups facilitate efficient coupling reactions, enabling the rapid assembly of diverse molecular scaffolds. This finding underscores its potential in accelerating drug discovery efforts, particularly in the context of emerging viral threats.

Another recent investigation, detailed in Organic & Biomolecular Chemistry, examined the compound's role in peptide modification. The researchers utilized 2-(Chloromethoxy)acetic Acid Ethyl Ester to introduce chloroalkoxy groups into peptide chains, thereby enhancing their stability and bioavailability. This approach could pave the way for the development of next-generation peptide-based therapeutics with improved pharmacokinetic properties.

From a safety and regulatory perspective, a 2024 report by the European Chemicals Agency (ECHA) provided updated toxicological data on 2-(Chloromethoxy)acetic Acid Ethyl Ester. The report confirmed its moderate acute toxicity but emphasized the need for proper handling due to its potential to cause skin and eye irritation. These findings are critical for researchers and manufacturers working with this compound, ensuring compliance with occupational health and safety standards.

Looking ahead, several research groups are investigating the potential of 2-(Chloromethoxy)acetic Acid Ethyl Ester in targeted drug delivery systems. Preliminary results suggest that its chemical structure could be modified to create pH-sensitive prodrugs, which would release active pharmaceutical ingredients selectively in diseased tissues. This innovative application could significantly improve the therapeutic index of various drugs while minimizing systemic side effects.

In conclusion, 2-(Chloromethoxy)acetic Acid Ethyl Ester continues to demonstrate its value as a multifunctional chemical intermediate in pharmaceutical research. The latest studies reinforce its importance in synthetic chemistry while uncovering new possibilities in drug development and delivery. As research progresses, this compound is likely to play an increasingly prominent role in addressing current challenges in medicinal chemistry and biomedicine.

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