Cas no 824414-06-4 (Ethyl 2-(piperazin-1-yl)propanoate)

Ethyl 2-(piperazin-1-yl)propanoate structure
824414-06-4 structure
Product Name:Ethyl 2-(piperazin-1-yl)propanoate
CAS No:824414-06-4
MF:C9H18N2O2
MW:186.251422405243
MDL:MFCD03410259
CID:715884
PubChem ID:2736463
Update Time:2025-11-01

Ethyl 2-(piperazin-1-yl)propanoate Chemical and Physical Properties

Names and Identifiers

    • Ethyl 2-(piperazin-1-yl)propanoate
    • 1-Piperazineaceticacid, a-methyl-, ethyl ester
    • 2-(PIPERAZIN-1-YL)PROPIONIC ACID ETHYL ESTER
    • ethyl 2-piperazin-1-ylpropanoate
    • 4-ethoxycarbonylethylpiperazine
    • ethyl 2-piperazin-1-ylpropionate
    • ethyl piperazin-1-ylpropionate
    • OR4192
    • PS-5076
    • CS-0456016
    • AKOS009158900
    • DTXSID90371377
    • SCHEMBL2110264
    • 824414-06-4
    • EN300-881744
    • A840336
    • LWPINFVZIFEBEG-UHFFFAOYSA-N
    • ZHB41406
    • rac 2-(piperazin-1-yl)-propionic acid ethyl ester
    • 2-(PIPERAZIN-1-YL)PROPIONICACIDETHYLESTER
    • ethyl 2-(piperazin-1-yl)propionate
    • Ethyl2-(piperazin-1-yl)propanoate
    • MDL: MFCD03410259
    • Inchi: 1S/C9H18N2O2/c1-3-13-9(12)8(2)11-6-4-10-5-7-11/h8,10H,3-7H2,1-2H3
    • InChI Key: LWPINFVZIFEBEG-UHFFFAOYSA-N
    • SMILES: O(CC)C(C(C)N1CCNCC1)=O

Computed Properties

  • Exact Mass: 186.13700
  • Monoisotopic Mass: 186.137
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 4
  • Heavy Atom Count: 13
  • Rotatable Bond Count: 4
  • Complexity: 167
  • 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: 0.3
  • Topological Polar Surface Area: 41.6?2

Experimental Properties

  • Color/Form: No data available
  • Density: 1.0±0.1 g/cm3
  • Melting Point: Not available
  • Boiling Point: 263.4±25.0 °C at 760 mmHg
  • Flash Point: 113.1±23.2 °C
  • Refractive Index: 1.464
  • PSA: 41.57000
  • LogP: 0.10990
  • Vapor Pressure: 0.0±0.5 mmHg at 25°C

Ethyl 2-(piperazin-1-yl)propanoate Customs Data

  • HS CODE:2933599090
  • Customs Data:

    China Customs Code:

    2933599090

    Overview:

    2933599090. Other compounds with pyrimidine ring in structure(Including other compounds with piperazine ring on the structure. VAT:17.0%. Tax refund rate:13.0%. Regulatory conditions:nothing. MFN tariff:6.5%. general tariff:20.0%

    Declaration elements:

    Product Name, component content, use to, Please indicate the appearance of Urotropine, 6- caprolactam please indicate the appearance, Signing date

    Summary:

    2933599090. other compounds containing a pyrimidine ring (whether or not hydrogenated) or piperazine ring in the structure. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

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Additional information on Ethyl 2-(piperazin-1-yl)propanoate

Recent Advances in the Study of Ethyl 2-(piperazin-1-yl)propanoate (CAS: 824414-06-4) and Its Applications in Chemical Biology and Medicine

Ethyl 2-(piperazin-1-yl)propanoate (CAS: 824414-06-4) is a compound of significant interest in the field of chemical biology and medicinal chemistry due to its versatile pharmacological properties and potential therapeutic applications. Recent studies have focused on its synthesis, structural optimization, and biological evaluation, shedding light on its mechanism of action and potential as a drug candidate. This research brief aims to summarize the latest findings related to this compound, providing insights into its current and future applications.

One of the key areas of research involving Ethyl 2-(piperazin-1-yl)propanoate is its role as a building block in the synthesis of more complex molecules. Recent publications have highlighted its utility in the development of novel piperazine derivatives, which are known for their broad-spectrum biological activities. For instance, a 2023 study published in the Journal of Medicinal Chemistry demonstrated the efficient synthesis of Ethyl 2-(piperazin-1-yl)propanoate and its subsequent conversion into a series of analogs with enhanced binding affinity for serotonin receptors. These findings underscore the compound's potential in the design of central nervous system (CNS) therapeutics.

In addition to its synthetic applications, Ethyl 2-(piperazin-1-yl)propanoate has been investigated for its direct pharmacological effects. A recent preclinical study explored its anti-inflammatory and analgesic properties, revealing that the compound exhibits significant activity in animal models of chronic pain. The study, conducted by researchers at a leading pharmaceutical institute, identified the compound's ability to modulate key inflammatory pathways, suggesting its potential as a non-opioid analgesic. These results were published in the European Journal of Pharmacology in early 2024, marking a notable advancement in pain management research.

Another emerging area of interest is the compound's application in targeted drug delivery systems. A 2023 paper in Advanced Drug Delivery Reviews discussed the use of Ethyl 2-(piperazin-1-yl)propanoate as a linker in prodrug formulations. The study demonstrated that the compound's chemical stability and biocompatibility make it an excellent candidate for conjugating therapeutic agents to targeting moieties, thereby improving drug efficacy and reducing off-target effects. This innovation has significant implications for the treatment of cancers and other diseases requiring precise drug delivery.

Despite these promising developments, challenges remain in the clinical translation of Ethyl 2-(piperazin-1-yl)propanoate-based therapies. Issues such as bioavailability, metabolic stability, and potential toxicity need to be addressed through further research. Ongoing studies are focusing on structural modifications to enhance the compound's pharmacokinetic profile while retaining its therapeutic benefits. Collaborative efforts between academic institutions and pharmaceutical companies are expected to accelerate progress in this area.

In conclusion, Ethyl 2-(piperazin-1-yl)propanoate (CAS: 824414-06-4) continues to be a molecule of great interest in chemical biology and medicinal research. Its versatility as a synthetic intermediate, combined with its direct pharmacological effects, positions it as a valuable tool for drug discovery and development. Future research will likely explore its applications in additional therapeutic areas, further solidifying its role in advancing modern medicine.

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