Cas no 1256667-56-7 ((3R)-1-(oxetan-3-yl)pyrrolidin-3-amine)

(3R)-1-(oxetan-3-yl)pyrrolidin-3-amine structure
1256667-56-7 structure
Product Name:(3R)-1-(oxetan-3-yl)pyrrolidin-3-amine
CAS No:1256667-56-7
MF:C7H14N2O
MW:142.198861598969
MDL:MFCD19690701
CID:1103305
PubChem ID:56604369
Update Time:2025-07-21

(3R)-1-(oxetan-3-yl)pyrrolidin-3-amine Chemical and Physical Properties

Names and Identifiers

    • (3R)-1-(3-oxetanyl)-3-Pyrrolidinamine
    • (3R)-1-(Oxetan-3-yl)pyrrolidin-3-amine
    • AS-52871
    • MFCD19690701
    • CS-0053349
    • PFMPDNZPMZCNHS-ZCFIWIBFSA-N
    • AKOS025311403
    • SCHEMBL1814882
    • P15820
    • 1256667-56-7
    • 3-Pyrrolidinamine, 1-(3-oxetanyl)-, (3R)-
    • (r)-1-(oxetan-3-yl)pyrrolidin-3-amine
    • (3R)-1-(oxetan-3-yl)pyrrolidin-3-amine
    • MDL: MFCD19690701
    • Inchi: 1S/C7H14N2O/c8-6-1-2-9(3-6)7-4-10-5-7/h6-7H,1-5,8H2/t6-/m1/s1
    • InChI Key: PFMPDNZPMZCNHS-ZCFIWIBFSA-N
    • SMILES: O1CC(C1)N1CC[C@H](C1)N

Computed Properties

  • Exact Mass: 142.110613074g/mol
  • Monoisotopic Mass: 142.110613074g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 1
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 10
  • Rotatable Bond Count: 1
  • Complexity: 125
  • Covalently-Bonded Unit Count: 1
  • Defined Atom Stereocenter Count: 1
  • Undefined Atom Stereocenter Count : 0
  • Defined Bond Stereocenter Count: 0
  • Undefined Bond Stereocenter Count: 0
  • XLogP3: -0.8
  • Topological Polar Surface Area: 38.5?2

Experimental Properties

  • Density: 1.2±0.1 g/cm3
  • Boiling Point: 214.1±35.0 °C at 760 mmHg
  • Flash Point: 83.3±25.9 °C
  • Vapor Pressure: 0.2±0.4 mmHg at 25°C

(3R)-1-(oxetan-3-yl)pyrrolidin-3-amine Security Information

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Additional information on (3R)-1-(oxetan-3-yl)pyrrolidin-3-amine

Recent Advances in the Study of (3R)-1-(oxetan-3-yl)pyrrolidin-3-amine (CAS: 1256667-56-7) in Chemical Biology and Pharmaceutical Research

The compound (3R)-1-(oxetan-3-yl)pyrrolidin-3-amine (CAS: 1256667-56-7) has recently emerged as a promising scaffold in chemical biology and pharmaceutical research. This molecule, characterized by its oxetane and pyrrolidine moieties, has attracted significant attention due to its potential applications in drug discovery, particularly in the development of novel therapeutics targeting central nervous system (CNS) disorders and infectious diseases. Recent studies have explored its synthetic accessibility, pharmacokinetic properties, and biological activities, positioning it as a versatile building block for medicinal chemistry.

One of the key findings in recent literature is the role of (3R)-1-(oxetan-3-yl)pyrrolidin-3-amine as a precursor in the synthesis of small-molecule inhibitors targeting enzymes such as kinases and proteases. Researchers have demonstrated that the oxetane ring enhances the metabolic stability of the compound while maintaining favorable solubility profiles. Additionally, the stereochemistry at the 3-position of the pyrrolidine ring has been shown to significantly influence binding affinity to biological targets, underscoring the importance of enantiomeric purity in its applications.

In a 2023 study published in the Journal of Medicinal Chemistry, (3R)-1-(oxetan-3-yl)pyrrolidin-3-amine was utilized as a key intermediate in the development of a new class of antiviral agents. The study highlighted its ability to improve the bioavailability of lead compounds through strategic modifications of its amine functionality. Furthermore, computational modeling and X-ray crystallography data revealed that the oxetane ring engages in unique hydrogen-bonding interactions with target proteins, providing insights for structure-based drug design.

Another significant advancement involves the application of this compound in the field of neuropharmacology. Preclinical studies have shown that derivatives of (3R)-1-(oxetan-3-yl)pyrrolidin-3-amine exhibit potent activity as modulators of neurotransmitter receptors, particularly those involved in dopamine and serotonin signaling. These findings suggest potential therapeutic avenues for treating psychiatric and neurodegenerative disorders, although further in vivo validation is required to assess efficacy and safety.

From a synthetic chemistry perspective, recent efforts have focused on optimizing the production of (3R)-1-(oxetan-3-yl)pyrrolidin-3-amine to meet the growing demand for high-purity material. Innovations in catalytic asymmetric synthesis and flow chemistry have enabled scalable and cost-effective manufacturing processes, addressing previous challenges related to yield and enantioselectivity. These advancements are expected to facilitate broader adoption of this compound in both academic and industrial research settings.

In conclusion, (3R)-1-(oxetan-3-yl)pyrrolidin-3-amine (CAS: 1256667-56-7) represents a valuable tool in modern drug discovery, with demonstrated utility across multiple therapeutic areas. Its unique structural features and favorable physicochemical properties make it an attractive candidate for further exploration. Future research directions may include the development of novel derivatives with enhanced selectivity and the investigation of its potential in combination therapies. As the field progresses, this compound is likely to play an increasingly important role in addressing unmet medical needs.

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