CAS 2292-84-4

3-Ethoxy-2,2-dimethylcyclobutanone

Description:

3-Ethoxy-2,2-dimethylcyclobutanone is an organic compound characterized by its unique cyclobutane ring structure, which is substituted with an ethoxy group and two methyl groups. This compound features a ketone functional group, contributing to its reactivity and potential applications in organic synthesis. The presence of the ethoxy group enhances its solubility in organic solvents, making it useful in various chemical reactions. Its molecular structure suggests that it may exhibit interesting physical properties, such as boiling and melting points that are influenced by the steric effects of the bulky dimethyl groups. Additionally, the compound may participate in nucleophilic addition reactions due to the electrophilic nature of the carbonyl carbon in the ketone group. While specific data on its toxicity and environmental impact may not be extensively documented, as with many organic compounds, proper handling and safety precautions are recommended. Overall, 3-Ethoxy-2,2-dimethylcyclobutanone is a valuable compound in the field of organic chemistry, particularly in the synthesis of more complex molecules.

Formula: C₈H₁₄O₂

InChI: InChI=1S/C8H14O2/c1-4-10-7-5-6(9)8(7,2)3/h7H,4-5H2,1-3H3

InChI key: InChIKey=CGOSXKKCMZZXNK-UHFFFAOYSA-N

SMILES: CC1(C)C(OCC)CC1=O

Synonyms:

• 2,2-Dimethyl-3-ethoxycyclobutanone
• 3-Ethoxy-2,2-dimethylcyclobutan-1-one
• 3-Ethoxy-2,2-dimethylcyclobutanone
• Cyclobutanone, 3-ethoxy-2,2-dimethyl-

3-Ethoxy-2,2-dimethylcyclobutanone

CAS: 2292-84-4

3-Ethoxy-2,2-dimethylcyclobutanone

Purity: 95%

Molecular weight: 142.20g/mol

Ref: 54-OR960827

3-ETHOXY-2,2-DIMETHYLCYCLOBUTANONE

CAS: 2292-84-4

Formula: C₈H₁₄O₂

Purity: 98%

Molecular weight: 142.198

Ref: 10-F502767

3-Ethoxy-2,2-dimethylcyclobutanone

CAS: 2292-84-4

3-Ethoxy-2,2-dimethylcyclobutanone is a cycloadduct that is produced by the reaction of an enol ether with dichloride. It is a nonpolar solvent used in chemistry and solvents. 3-Ethoxy-2,2-dimethylcyclobutanone is also an oxygenated compound and can be used as a nucleophile in reactions. The regioselectivity of 3-ethoxy-2,2-dimethylcyclobutanone depends on the type of reaction that it is involved in; however, it has been shown to preferentially form the cyclohexanone product in most cases.

Formula: C₈H₁₄O₂

Purity: Min. 95%

Molecular weight: 142.2 g/mol

Ref: 3D-CAA29284