CAS 30830-25-2

3α-Methoxycyclobutanone

Description:

3α-Methoxycyclobutanone is a cyclic ketone characterized by its four-membered cyclobutane ring structure, which is substituted with a methoxy group and a carbonyl functional group. This compound typically exhibits a unique set of physical and chemical properties due to its ring strain and functional groups. It is generally a colorless to pale yellow liquid or solid, depending on the temperature and purity. The presence of the methoxy group contributes to its reactivity, making it a potential candidate for various organic synthesis applications. The compound may participate in nucleophilic addition reactions due to the electrophilic nature of the carbonyl carbon. Additionally, its structural features may influence its solubility in organic solvents and its stability under different conditions. As with many organic compounds, safety precautions should be taken when handling 3α-Methoxycyclobutanone, as it may pose health risks if ingested or inhaled. Overall, this compound is of interest in the field of organic chemistry for its unique structure and potential applications in synthesis.

Formula: C₅H₈O₂

Synonyms:

• Cyclobutanone, 3-methoxy-
• 3-methoxycyclobutan-1-one
• 3α-Methoxycyclobutanone
• 3-Methoxycyclobutanon

Cyclobutanone, 3-methoxy-

CAS: 30830-25-2

Formula: C₅H₈O₂

Purity: 98%

Color and Shape: Liquid

Molecular weight: 100.1158

Ref: IN-DA0031G7

3-Methoxycyclobutan-1-one

CAS: 30830-25-2

3-Methoxycyclobutan-1-one

Purity: 98%

Molecular weight: 100.12g/mol

Ref: 54-OR949039

3-Methoxycyclobutanone

CAS: 30830-25-2

Formula: C₅H₈O₂

Purity: 98%

Color and Shape: Liquid

Molecular weight: 100.117

Ref: 10-F457700

3-Methoxycyclobutan-1-one

CAS: 30830-25-2

3-Methoxycyclobutan-1-one (3MCO) is an electron donor and is capable of undergoing electrochemical oxidation. 3MCO has been shown to oxidize electron acceptors, such as hydrocarbons, and transfer the electrons to a second electron acceptor. The mechanism of this process is thought to be a three-electron transfer, which is also known as a "polycyclic" reaction. 3MCO has also been shown to have anti-inflammatory properties by inhibiting prostaglandin synthesis in mice with lung cancer.

Formula: C₅H₈O₂

Purity: Min. 95%

Molecular weight: 100.12 g/mol

Ref: 3D-FBA83025