Cas no 922500-97-8 (3,3-dimethoxyoxetane)

3,3-Dimethoxyoxetane is a versatile heterocyclic compound characterized by its oxetane ring functionalized with two methoxy groups at the 3-position. This structure imparts high reactivity, making it a valuable intermediate in organic synthesis, particularly for ring-opening polymerizations and cross-linking reactions. Its strained oxetane ring enhances its utility in forming polyethers and other polymeric materials with tailored properties. The dimethoxy substitution further improves solubility and stability, facilitating handling and storage. Applications include adhesives, coatings, and specialty resins where controlled polymerization and enhanced material performance are required. Its balanced reactivity and functional group compatibility make it a preferred choice in advanced chemical synthesis.
3,3-dimethoxyoxetane structure
3,3-dimethoxyoxetane structure
Product Name:3,3-dimethoxyoxetane
CAS No:922500-97-8
MF:C5H10O3
MW:118.131102085114
MDL:MFCD12545828
CID:740877
PubChem ID:15947203
Update Time:2025-06-13

3,3-dimethoxyoxetane Chemical and Physical Properties

Names and Identifiers

    • Oxetane, 3,3-dimethoxy-
    • 3,3-DIMETHOXYOXETANE
    • 3,3-Dimethoxy-oxetane
    • Oxetane,3,3-dimethoxy
    • AKOS015996228
    • AS-32685
    • SY067909
    • CS-0057692
    • MFCD12545828
    • XLB50097
    • PB28447
    • 922500-97-8
    • DTXSID20580218
    • DB-347772
    • 3,3-dimethoxyoxetane
    • MDL: MFCD12545828
    • Inchi: 1S/C5H10O3/c1-6-5(7-2)3-8-4-5/h3-4H2,1-2H3
    • InChI Key: OXBBCZDEGXLJCJ-UHFFFAOYSA-N
    • SMILES: O1CC(C1)(OC)OC

Computed Properties

  • Exact Mass: 118.06300
  • Monoisotopic Mass: 118.062994177g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 3
  • Heavy Atom Count: 8
  • Rotatable Bond Count: 2
  • Complexity: 71.7
  • 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: -0.5
  • Topological Polar Surface Area: 27.7?2

Experimental Properties

  • PSA: 27.69000
  • LogP: 0.00570

3,3-dimethoxyoxetane Customs Data

  • HS CODE:2932999099
  • Customs Data:

    China Customs Code:

    2932999099

    Overview:

    2932999099. Other heterocyclic compounds containing only oxygen 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

    Summary:

    2932999099. other heterocyclic compounds with oxygen hetero-atom(s) only. VAT:17.0%. Tax rebate rate:13.0%. . MFN tariff:6.5%. General tariff:20.0%

3,3-dimethoxyoxetane Pricemore >>

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Alichem
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Apollo Scientific
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abcr
AB304764-500 mg
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abcr
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Additional information on 3,3-dimethoxyoxetane

Recent Advances in the Application of 3,3-Dimethoxyoxetane (CAS: 922500-97-8) in Chemical Biology and Pharmaceutical Research

3,3-Dimethoxyoxetane (CAS: 922500-97-8) has emerged as a versatile building block in chemical biology and pharmaceutical research due to its unique structural and reactivity properties. Recent studies have highlighted its potential in the synthesis of novel bioactive molecules, drug delivery systems, and polymer chemistry. This research brief aims to summarize the latest findings and applications of 3,3-dimethoxyoxetane, providing insights into its role in advancing the field.

One of the most significant developments involves the use of 3,3-dimethoxyoxetane as a precursor for the synthesis of oxetane-containing compounds, which are known for their enhanced metabolic stability and bioavailability. A 2023 study published in the Journal of Medicinal Chemistry demonstrated the successful incorporation of 3,3-dimethoxyoxetane into a series of kinase inhibitors, resulting in improved pharmacokinetic profiles. The study utilized advanced computational modeling and high-throughput screening to identify optimal synthetic pathways, underscoring the compound's utility in drug design.

In addition to its role in small-molecule therapeutics, 3,3-dimethoxyoxetane has been explored for its applications in polymer science. Researchers at MIT recently reported the development of a new class of biodegradable polymers incorporating 3,3-dimethoxyoxetane as a key monomer. These polymers exhibited remarkable mechanical properties and controlled degradation rates, making them promising candidates for medical implants and tissue engineering. The study, published in Advanced Materials, also highlighted the compound's compatibility with ring-opening polymerization techniques, further expanding its potential applications.

Another area of interest is the use of 3,3-dimethoxyoxetane in prodrug strategies. A 2024 study in Chemical Communications detailed the design of a prodrug system where 3,3-dimethoxyoxetane served as a masking group for a potent anticancer agent. The prodrug demonstrated selective activation in tumor microenvironments, minimizing off-target effects and improving therapeutic efficacy. This approach represents a significant advancement in targeted drug delivery, with potential implications for cancer treatment.

Despite these promising developments, challenges remain in the large-scale synthesis and purification of 3,3-dimethoxyoxetane. Recent efforts have focused on optimizing synthetic protocols to enhance yield and purity. A collaborative study between academia and industry, published in Organic Process Research & Development, proposed a scalable route using continuous flow chemistry, which reduced reaction times and improved overall efficiency. These advancements are critical for facilitating the broader adoption of 3,3-dimethoxyoxetane in industrial applications.

In conclusion, 3,3-dimethoxyoxetane (CAS: 922500-97-8) continues to attract attention as a valuable tool in chemical biology and pharmaceutical research. Its applications span drug design, polymer science, and prodrug development, driven by its unique chemical properties. Ongoing research aims to address synthetic challenges and explore new avenues for its use, positioning 3,3-dimethoxyoxetane as a key player in the future of medicinal chemistry and materials science.

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