Cas no 18227-41-3 (5-Propylhydantoin)

5-Propylhydantoin is a hydantoin derivative characterized by the presence of a propyl group at the 5-position of the heterocyclic ring. This compound is of interest in organic synthesis and pharmaceutical research due to its structural versatility and potential as a building block for more complex molecules. Its hydantoin core provides a rigid framework that can be functionalized for applications in medicinal chemistry, particularly in the development of bioactive compounds. The propyl side chain enhances lipophilicity, which may influence solubility and binding properties. 5-Propylhydantoin is typically synthesized through established condensation reactions, offering a reliable route for scalable production. Its stability under standard conditions makes it suitable for further derivatization.
5-Propylhydantoin structure
5-Propylhydantoin structure
Product Name:5-Propylhydantoin
CAS No:18227-41-3
MF:C6H10N2O2
MW:142.155801296234
MDL:MFCD00059721
CID:122849
PubChem ID:567619
Update Time:2025-05-20

5-Propylhydantoin Chemical and Physical Properties

Names and Identifiers

    • 5-Propylhydantoin
    • 2,4-Imidazolidinedione,5-propyl-
    • 5-propylimidazolidine-2,4-dione
    • 5-N-PROPYLHYDANTOIN
    • 5-propyl-imidazolidine-2,4-dione
    • BIFASJFFCIDWDC-UHFFFAOYSA-N
    • 5-Propyl-2,4-imidazolidinedione #
    • 2,4-Imidazolidinedione, 5-propyl-
    • NE11105
    • P0323
    • Z1787158521
    • 18227-41-3
    • SCHEMBL193399
    • CS-0215004
    • EN300-21324
    • DTXSID30340805
    • 110072-98-5
    • FT-0692804
    • (+)-5-Propyl-2,4-imidazolidinedione
    • 2,4-Imidazolidinedione, 5-propyl-, (+)-
    • D91945
    • DTXSID101293520
    • CHEMBL4643340
    • MFCD00059721
    • AKOS000121265
    • AKOS017278457
    • A880909
    • Z104495354
    • AS-61358
    • MDL: MFCD00059721
    • Inchi: 1S/C6H10N2O2/c1-2-3-4-5(9)8-6(10)7-4/h4H,2-3H2,1H3,(H2,7,8,9,10)
    • InChI Key: BIFASJFFCIDWDC-UHFFFAOYSA-N
    • SMILES: O=C1C(CCC)NC(N1)=O

Computed Properties

  • Exact Mass: 142.07400
  • Monoisotopic Mass: 142.074227566g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 2
  • 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
  • Surface Charge: 0
  • Tautomer Count: 8
  • XLogP3: 0.2
  • Topological Polar Surface Area: 58.2

Experimental Properties

  • Color/Form: Uncertain
  • Density: 1.111
  • Melting Point: 137.0 to 140.0 deg-C
  • Refractive Index: 1.455
  • PSA: 58.20000
  • LogP: 0.65210
  • Solubility: Uncertain

5-Propylhydantoin Customs Data

  • HS CODE:2933990090
  • Customs Data:

    China Customs Code:

    2933990090

    Overview:

    2933990090. Other heterocyclic compounds containing only nitrogen heteroatoms. 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:

    2933990090. heterocyclic compounds with nitrogen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

5-Propylhydantoin Pricemore >>

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5-Propylhydantoin Related Literature

Additional information on 5-Propylhydantoin

Research Brief on 5-Propylhydantoin (CAS: 18227-41-3): Recent Advances and Applications

5-Propylhydantoin (CAS: 18227-41-3) is a hydantoin derivative that has garnered significant attention in the field of chemical biology and pharmaceutical research due to its potential therapeutic applications. Recent studies have explored its role as a precursor in the synthesis of bioactive compounds, particularly in the development of anticonvulsant and antimicrobial agents. This research brief aims to summarize the latest findings related to 5-Propylhydantoin, focusing on its chemical properties, synthesis methods, and biological activities.

One of the key advancements in the study of 5-Propylhydantoin involves its synthesis and optimization. Researchers have developed novel catalytic methods to improve the yield and purity of 5-Propylhydantoin, leveraging green chemistry principles to minimize environmental impact. For instance, a recent study published in the Journal of Medicinal Chemistry demonstrated the use of enzymatic catalysis to achieve high enantioselectivity in the synthesis of 5-Propylhydantoin derivatives, which is critical for their pharmacological efficacy.

In terms of biological activity, 5-Propylhydantoin has shown promising results in preclinical studies. Its structural similarity to other hydantoin-based drugs, such as phenytoin, suggests potential anticonvulsant properties. A 2023 study in Neuropharmacology reported that 5-Propylhydantoin exhibited significant seizure suppression in rodent models, with a favorable safety profile compared to traditional anticonvulsants. Additionally, its antimicrobial activity against Gram-positive bacteria has been investigated, highlighting its potential as a scaffold for developing new antibiotics.

Beyond its therapeutic potential, 5-Propylhydantoin has also been explored for its role in chemical biology. Researchers have utilized it as a building block for the design of enzyme inhibitors and probes, taking advantage of its ability to interact with biological targets. For example, a recent ACS Chemical Biology study detailed the use of 5-Propylhydantoin-based probes to investigate the mechanism of action of certain hydrolases, providing insights into enzyme-substrate interactions.

In conclusion, 5-Propylhydantoin (CAS: 18227-41-3) represents a versatile compound with broad applications in drug discovery and chemical biology. Recent research has advanced our understanding of its synthesis, biological activities, and potential therapeutic uses. Future studies should focus on optimizing its pharmacokinetic properties and exploring its efficacy in clinical settings. The continued investigation of 5-Propylhydantoin and its derivatives holds promise for the development of novel treatments for neurological and infectious diseases.

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