Cas no 95361-30-1 (2,4-Imidazolidinedione,5-(2-naphthalenyl)-)

2,4-Imidazolidinedione,5-(2-naphthalenyl)- is a heterocyclic organic compound featuring an imidazolidinedione core substituted with a naphthalenyl group at the 5-position. This structure imparts unique chemical properties, making it valuable for applications in pharmaceutical and agrochemical research. The naphthalene moiety enhances aromatic interactions, potentially improving binding affinity in bioactive molecules. Its rigid framework offers stability, while the imidazolidinedione group provides reactivity for further functionalization. The compound is of interest in the synthesis of novel therapeutic agents, particularly in the development of enzyme inhibitors or receptor modulators. High purity grades ensure consistent performance in research and industrial applications. Proper handling and storage are recommended due to its sensitivity to light and moisture.
2,4-Imidazolidinedione,5-(2-naphthalenyl)- structure
95361-30-1 structure
Product Name:2,4-Imidazolidinedione,5-(2-naphthalenyl)-
CAS No:95361-30-1
MF:C13H10N2O2
MW:226.230702877045
CID:796781
PubChem ID:11229868
Update Time:2025-05-27

2,4-Imidazolidinedione,5-(2-naphthalenyl)- Chemical and Physical Properties

Names and Identifiers

    • 2,4-Imidazolidinedione,5-(2-naphthalenyl)-
    • 5-(2-Naphthyl)-2,4-imidazolidinedione
    • 2-(1-Naphthyl)-4-thiophencarbonsaeure
    • 4-(2-naphthyl)-2,5-imidazolinedione
    • 5-(1-naphthyl)thiophene-2-carboxylic acid
    • 5-(2-Naphthylhydantoin)
    • 5-naphthalen-1-yl-thiophene-2-carboxylic acid
    • 5-naphthalen-2-yl-imidazolidine-2,4-dione
    • 5-naphthylthiophene-2-carboxylic acid
    • 5-(2-Naphthalenyl)hydantoin
    • DL-5-(2-Naphthyl)hydantoin
    • 5-(2-naphthyl) hydantoin
    • SCHEMBL2829814
    • AKOS009122529
    • 95361-30-1
    • 5-(NAPHTHALEN-2-YL)IMIDAZOLIDINE-2,4-DIONE
    • HLGCUXIRWKRNJF-UHFFFAOYSA-N
    • Inchi: 1S/C13H10N2O2/c16-12-11(14-13(17)15-12)10-6-5-8-3-1-2-4-9(8)7-10/h1-7,11H,(H2,14,15,16,17)
    • InChI Key: HLGCUXIRWKRNJF-UHFFFAOYSA-N
    • SMILES: O=C1C(C2C=CC3C=CC=CC=3C=2)NC(N1)=O

Computed Properties

  • Exact Mass: 226.07400
  • Monoisotopic Mass: 226.074227566g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 17
  • Rotatable Bond Count: 1
  • Complexity: 342
  • 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: 1.7
  • Topological Polar Surface Area: 58.2?2

Experimental Properties

  • Density: 1.314±0.06 g/cm3 (20 oC 760 Torr),
  • Solubility: Very slightly soluble (0.1 g/l) (25 o C),
  • PSA: 65.18000
  • LogP: 1.63620

2,4-Imidazolidinedione,5-(2-naphthalenyl)- Pricemore >>

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2,4-Imidazolidinedione,5-(2-naphthalenyl)- Related Literature

Additional information on 2,4-Imidazolidinedione,5-(2-naphthalenyl)-

2,4-Imidazolidinedione,5-(2-naphthalenyl)-: A Comprehensive Overview

The compound CAS No. 95361-30-1, also known as 2,4-imidazolidinedione,5-(2-naphthalenyl)-, is a significant molecule in the field of organic chemistry and pharmacology. This compound belongs to the class of imidazolidinediones, which are heterocyclic compounds with a five-membered ring containing two nitrogen atoms and two ketone groups. The presence of the naphthalene group at the 5-position of the imidazolidinedione ring introduces unique electronic and structural properties that make this compound a subject of interest in various research domains.

Recent studies have highlighted the potential of 2,4-imidazolidinedione,5-(2-naphthalenyl)- in drug discovery and development. Its structure allows for versatile interactions with biological targets, making it a promising candidate for therapeutic applications. For instance, researchers have explored its ability to act as a scaffold for designing inhibitors of certain enzymes or receptors involved in disease pathways. The naphthalene moiety contributes to the molecule's hydrophobicity, enhancing its ability to penetrate cellular membranes and interact with target proteins.

In addition to its pharmacological applications, CAS No. 95361-30-1 has also been investigated for its role in materials science. The compound's structural rigidity and conjugated system make it a potential candidate for use in organic electronics or as a component in advanced materials. Recent advancements in computational chemistry have enabled researchers to predict the electronic properties of this compound more accurately, paving the way for its integration into next-generation technologies.

The synthesis of 2,4-imidazolidinedione,5-(2-naphthalenyl)- involves a series of well-established organic reactions. Starting from naphthalene derivatives, chemists employ methods such as nucleophilic substitution or condensation reactions to construct the imidazolidinedione core. The optimization of these synthetic routes has been a focus of recent research efforts, with the aim of improving yield and purity while reducing costs.

From an environmental perspective, understanding the fate and transport of CAS No. 95361-30-1 in natural systems is crucial for assessing its potential impact on ecosystems. Studies have shown that the compound exhibits moderate biodegradability under certain conditions, though further research is needed to fully characterize its environmental behavior.

In conclusion, 2,4-imidazolidinedione,5-(2-naphthalenyl)-, or CAS No. 95361-30-1, is a multifaceted compound with applications spanning drug discovery, materials science, and environmental chemistry. Its unique structure and functional groups make it a valuable tool for researchers across various disciplines. As ongoing studies continue to uncover new insights into its properties and potential uses, this compound is poised to play an increasingly important role in both academic and industrial settings.

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