Cas no 30830-25-2 (3-methoxycyclobutan-1-one)

3-Methoxycyclobutan-1-one is a versatile cyclic ketone derivative characterized by its methoxy-substituted cyclobutanone structure. This compound is of interest in synthetic organic chemistry due to its strained four-membered ring, which offers unique reactivity for ring-opening and functionalization reactions. The methoxy group enhances its utility as a building block for pharmaceuticals, agrochemicals, and specialty materials by providing a handle for further derivatization. Its stability under mild conditions and compatibility with a range of reagents make it a practical intermediate for constructing complex molecular architectures. Researchers value this compound for its potential in stereoselective synthesis and as a precursor to bioactive molecules.
3-methoxycyclobutan-1-one structure
3-methoxycyclobutan-1-one structure
Product Name:3-methoxycyclobutan-1-one
CAS No:30830-25-2
MF:C5H8O2
MW:100.115821838379
MDL:MFCD20266830
CID:1006217
PubChem ID:13808253
Update Time:2025-10-31

3-methoxycyclobutan-1-one Chemical and Physical Properties

Names and Identifiers

    • 3Α-METHOXYCYCLOBUTANONE
    • 3-Methoxycyclobutanon
    • 3-methoxycyclobutanone
    • 3-methoxycyclobutan-1-one
    • SB11270
    • Cyclobutanone, 3-methoxy-
    • 30830-25-2
    • CS-0051289
    • A876082
    • 3alpha-Methoxycyclobutanone
    • AKOS015711577
    • EN300-121706
    • BS-12784
    • SY098914
    • P12741
    • SCHEMBL16885218
    • MFCD20266830
    • MDL: MFCD20266830
    • Inchi: 1S/C5H8O2/c1-7-5-2-4(6)3-5/h5H,2-3H2,1H3
    • InChI Key: LZKSSLYIICHJEO-UHFFFAOYSA-N
    • SMILES: O(C)C1CC(C1)=O

Computed Properties

  • Exact Mass: 100.052429494g/mol
  • Monoisotopic Mass: 100.052429494g/mol
  • Isotope Atom Count: 0
  • Hydrogen Bond Donor Count: 0
  • Hydrogen Bond Acceptor Count: 2
  • Heavy Atom Count: 7
  • Rotatable Bond Count: 1
  • Complexity: 80.1
  • 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: -0.4
  • Topological Polar Surface Area: 26.3?2

Experimental Properties

  • Density: 1.03±0.1 g/cm3 (20 oC 760 Torr),
  • Boiling Point: 51 oC (16 Torr)
  • Flash Point: 41.9±18.9 oC,
  • Refractive Index: 1.429 (589.3 nm 20 oC)
  • Solubility: Soluble (110 g/l) (25 o C),

3-methoxycyclobutan-1-one Pricemore >>

Related Categories No. Product Name Cas No. Purity Specification Price update time Inquiry
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Additional information on 3-methoxycyclobutan-1-one

3-Methoxycyclobutan-1-one

The compound 3-Methoxycyclobutan-1-one (CAS No: 30830-25-2) is a cyclic ketone derivative with a methoxy group attached at the third position of the cyclobutane ring. This compound has been the subject of extensive research due to its unique chemical properties and potential applications in various fields, including organic synthesis, pharmaceuticals, and materials science.

Recent studies have highlighted the importance of cyclobutanones in the development of bioactive molecules. The methoxy group in 3-Methoxycyclobutan-1-one introduces additional electronic effects, making it a valuable building block for constructing complex molecular architectures. Researchers have explored its use in the synthesis of natural product analogs, where its strained ring system contributes to interesting stereochemical outcomes.

In terms of synthesis, 3-Methoxycyclobutan-1-one can be prepared via various methods, including the oxidation of cyclopropane derivatives or through enolate chemistry. These methods have been optimized to achieve high yields and selectivity, making it accessible for large-scale applications.

The compound's reactivity is another area of active investigation. Its strained cyclobutane ring makes it highly susceptible to ring-opening reactions under specific conditions, which has been exploited in the development of novel catalytic processes. For instance, recent work has demonstrated its utility in asymmetric catalysis, where it serves as a chiral auxiliary to induce enantioselectivity in key transformations.

Beyond its chemical synthesis applications, 3-Methoxycyclobutan-1-one has shown promise in biological systems. Preclinical studies suggest that it may exhibit anti-inflammatory and antioxidant properties, opening avenues for its potential use in drug discovery programs targeting chronic diseases such as neurodegenerative disorders and cardiovascular conditions.

Moreover, the compound's photophysical properties have been studied for applications in optoelectronics. Its ability to absorb and emit light at specific wavelengths makes it a candidate for use in organic light-emitting diodes (OLEDs) and other advanced materials.

In conclusion, 3-Methoxycyclobutan-1-one (CAS No: 30830-25-2) is a versatile compound with a wide range of applications across multiple disciplines. Its unique structure and reactivity continue to inspire innovative research directions, solidifying its position as an important molecule in contemporary chemistry.

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