Cas no 932742-86-4 (4-(5-Methyl-1,2,4-oxadiazol-3-yl)benzenemethanamine)

4-(5-Methyl-1,2,4-oxadiazol-3-yl)benzenemethanamine is a heterocyclic aromatic compound featuring a 1,2,4-oxadiazole core substituted with a methyl group at the 5-position and a benzenemethanamine moiety at the 3-position. This structure imparts unique reactivity and potential utility in pharmaceutical and agrochemical applications, particularly as a versatile intermediate in medicinal chemistry. The oxadiazole ring enhances metabolic stability, while the benzenemethanamine group offers functionalization opportunities for further derivatization. Its well-defined synthetic route and high purity make it suitable for research in drug discovery and material science. The compound’s balanced lipophilicity and electronic properties contribute to its relevance in designing bioactive molecules.
4-(5-Methyl-1,2,4-oxadiazol-3-yl)benzenemethanamine structure
932742-86-4 structure
Product Name:4-(5-Methyl-1,2,4-oxadiazol-3-yl)benzenemethanamine
CAS No:932742-86-4
MF:C10H11N3O
MW:189.213841676712
CID:69554
PubChem ID:28064824
Update Time:2025-11-02

4-(5-Methyl-1,2,4-oxadiazol-3-yl)benzenemethanamine Chemical and Physical Properties

Names and Identifiers

    • (4-(5-Methyl-1,2,4-oxadiazol-3-yl)phenyl)methanamine
    • [4-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]methanamine
    • 4-(5-Methyl-1,2,4-oxadiazol-3-yl)benzylamine
    • 1-[4-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]methanamine(SALTDATA: 1HCl 0.4H2O)
    • 4-(5-METHYL-1,2,4-OXADIAZOL-3-YL)-BENZENEMETHANAMINE
    • DTXSID40650987
    • SCHEMBL15307622
    • 932742-86-4
    • EN300-1721613
    • AKOS006326914
    • FT-0735118
    • 1-[4-(5-methyl-1,2,4-oxadiazol-3-yl)phenyl]methanamine
    • 4-(5-Methyl-1,2,4-oxadiazol-3-yl)benzenemethanamine
    • MDL: MFCD09752178
    • Inchi: 1S/C10H11N3O/c1-7-12-10(13-14-7)9-4-2-8(6-11)3-5-9/h2-5H,6,11H2,1H3
    • InChI Key: LSTDWUOSWUXAJV-UHFFFAOYSA-N
    • SMILES: O1C(C)=NC(C2C=CC(CN)=CC=2)=N1

Computed Properties

  • Exact Mass: 189.09000
  • Monoisotopic Mass: 189.090211983g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 14
  • Rotatable Bond Count: 2
  • Complexity: 180
  • 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: 1.2
  • Topological Polar Surface Area: 64.9?2

Experimental Properties

  • PSA: 64.94000
  • LogP: 2.20400

4-(5-Methyl-1,2,4-oxadiazol-3-yl)benzenemethanamine Pricemore >>

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Additional information on 4-(5-Methyl-1,2,4-oxadiazol-3-yl)benzenemethanamine

Recent Advances in the Study of 4-(5-Methyl-1,2,4-oxadiazol-3-yl)benzenemethanamine (CAS: 932742-86-4)

The compound 4-(5-Methyl-1,2,4-oxadiazol-3-yl)benzenemethanamine (CAS: 932742-86-4) has recently garnered significant attention in the field of chemical biology and medicinal chemistry due to its potential applications in drug discovery and development. This research brief aims to summarize the latest findings related to this compound, focusing on its synthesis, biological activity, and therapeutic potential.

Recent studies have highlighted the versatility of 4-(5-Methyl-1,2,4-oxadiazol-3-yl)benzenemethanamine as a key intermediate in the synthesis of novel bioactive molecules. The oxadiazole ring, a prominent feature of this compound, is known for its stability and ability to participate in hydrogen bonding, making it a valuable scaffold in medicinal chemistry. Researchers have successfully utilized this compound to develop inhibitors targeting various enzymes, including kinases and proteases, which are implicated in numerous diseases.

One notable study published in the Journal of Medicinal Chemistry demonstrated the efficacy of derivatives of 4-(5-Methyl-1,2,4-oxadiazol-3-yl)benzenemethanamine in modulating the activity of protein kinases involved in cancer progression. The study employed a combination of molecular docking and in vitro assays to identify potent inhibitors with high selectivity and low cytotoxicity. These findings suggest that this compound could serve as a promising lead for the development of targeted cancer therapies.

In addition to its applications in oncology, 4-(5-Methyl-1,2,4-oxadiazol-3-yl)benzenemethanamine has also been investigated for its potential in treating neurological disorders. A recent preprint on bioRxiv reported that derivatives of this compound exhibited neuroprotective effects in models of Alzheimer's disease. The researchers attributed these effects to the compound's ability to inhibit amyloid-beta aggregation and reduce oxidative stress in neuronal cells.

Despite these promising results, challenges remain in optimizing the pharmacokinetic properties of 4-(5-Methyl-1,2,4-oxadiazol-3-yl)benzenemethanamine derivatives. Issues such as poor solubility and metabolic instability have been identified as potential barriers to clinical translation. Ongoing research is focused on structural modifications to enhance the drug-like properties of these compounds while retaining their biological activity.

In conclusion, 4-(5-Methyl-1,2,4-oxadiazol-3-yl)benzenemethanamine (CAS: 932742-86-4) represents a valuable scaffold in medicinal chemistry with diverse therapeutic potential. Continued research efforts are expected to yield novel derivatives with improved efficacy and safety profiles, paving the way for their eventual clinical application.

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