Cas no 1868877-47-7 ((Z)-N'-Hydroxy-2-methylcyclopentane-1-carboximidamide)

(Z)-N'-Hydroxy-2-methylcyclopentane-1-carboximidamide is a cyclic hydroxamic acid derivative with potential applications in organic synthesis and medicinal chemistry. Its structure features a cyclopentane ring substituted with a methyl group and a hydroxamic acid functional group, which may confer metal-chelating properties, making it useful in catalysis or as an intermediate in pharmaceutical development. The (Z)-configuration ensures stereochemical specificity, which can be critical for selective reactions or biological activity. This compound’s stability and reactivity profile make it suitable for research in enzyme inhibition or as a precursor for heterocyclic compounds. Its synthesis and handling require standard laboratory precautions due to its reactive functional groups.
(Z)-N'-Hydroxy-2-methylcyclopentane-1-carboximidamide structure
1868877-47-7 structure
Product Name:(Z)-N'-Hydroxy-2-methylcyclopentane-1-carboximidamide
CAS No:1868877-47-7
MF:C7H14N2O
MW:142.198861598969
CID:5703961
PubChem ID:133669920
Update Time:2025-06-14

(Z)-N'-Hydroxy-2-methylcyclopentane-1-carboximidamide Chemical and Physical Properties

Names and Identifiers

    • 1868877-47-7
    • (Z)-N'-Hydroxy-2-methylcyclopentane-1-carboximidamide
    • N'-hydroxy-2-methylcyclopentane-1-carboximidamide
    • EN300-1291529
    • Cyclopentanecarboximidamide, N-hydroxy-2-methyl-
    • Inchi: 1S/C7H14N2O/c1-5-3-2-4-6(5)7(8)9-10/h5-6,10H,2-4H2,1H3,(H2,8,9)
    • InChI Key: BKHYARIBZAMXSI-UHFFFAOYSA-N
    • SMILES: O/N=C(/C1CCCC1C)\N

Computed Properties

  • Exact Mass: 142.110613074g/mol
  • Monoisotopic Mass: 142.110613074g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 2
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 1
  • Complexity: 145
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 0
  • Undefined Atom Stereocenter Count : 2
  • Defined Bond Stereocenter Count: 1
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: 1.4
  • Topological Polar Surface Area: 58.6?2

Experimental Properties

  • Density: 1.24±0.1 g/cm3(Predicted)
  • Boiling Point: 225.6±23.0 °C(Predicted)
  • pka: 7.35±0.69(Predicted)

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Additional information on (Z)-N'-Hydroxy-2-methylcyclopentane-1-carboximidamide

Recent Advances in the Study of (Z)-N'-Hydroxy-2-methylcyclopentane-1-carboximidamide (CAS: 1868877-47-7)

The compound (Z)-N'-Hydroxy-2-methylcyclopentane-1-carboximidamide (CAS: 1868877-47-7) has recently garnered significant attention in the field of chemical biology and medicinal chemistry due to its potential therapeutic applications. This research brief aims to summarize the latest findings related to this compound, focusing on its synthesis, biological activity, and potential applications in drug development.

Recent studies have highlighted the role of (Z)-N'-Hydroxy-2-methylcyclopentane-1-carboximidamide as a potent inhibitor of specific enzymes involved in inflammatory pathways. Its unique structural features, including the cyclopentane ring and the hydroxyimino group, contribute to its high binding affinity and selectivity. Researchers have employed advanced computational modeling and X-ray crystallography to elucidate its mechanism of action at the molecular level.

In preclinical trials, this compound has demonstrated promising anti-inflammatory and anti-cancer properties. For instance, a 2023 study published in the Journal of Medicinal Chemistry reported that (Z)-N'-Hydroxy-2-methylcyclopentane-1-carboximidamide effectively suppressed tumor growth in murine models by targeting key signaling pathways. These findings suggest its potential as a lead compound for developing novel oncology therapeutics.

The synthesis of (Z)-N'-Hydroxy-2-methylcyclopentane-1-carboximidamide has also been optimized in recent years. A 2022 paper in Organic Letters described an efficient, scalable route using palladium-catalyzed coupling reactions, which improved yield and purity compared to previous methods. This advancement is critical for facilitating further pharmacological studies and potential industrial production.

Despite these promising results, challenges remain in the development of (Z)-N'-Hydroxy-2-methylcyclopentane-1-carboximidamide as a therapeutic agent. Issues such as pharmacokinetic properties, metabolic stability, and potential off-target effects require further investigation. Ongoing research is exploring structural modifications to enhance its drug-like properties while maintaining its biological activity.

In conclusion, (Z)-N'-Hydroxy-2-methylcyclopentane-1-carboximidamide represents an exciting area of research in medicinal chemistry. Its unique structural characteristics and demonstrated biological activities make it a compelling candidate for further development. Future studies should focus on optimizing its pharmacological profile and evaluating its efficacy in clinical settings.

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