CAS 1080636-35-6

3-(2-Chlorophenyl)cyclobutanone

Description:

3-(2-Chlorophenyl)cyclobutanone is an organic compound characterized by its cyclobutanone structure, which features a four-membered carbon ring with a ketone functional group. The presence of a 2-chlorophenyl group indicates that a chlorine atom is substituted on the phenyl ring at the second position, influencing the compound's reactivity and physical properties. This compound typically exhibits a solid state at room temperature and may have moderate solubility in organic solvents, depending on the specific solvent's polarity. Its molecular structure suggests potential applications in organic synthesis and medicinal chemistry, particularly in the development of pharmaceuticals or agrochemicals. The chlorine substituent can enhance biological activity or alter the compound's interaction with biological targets. As with many organic compounds, safety precautions should be taken when handling 3-(2-Chlorophenyl)cyclobutanone, as it may pose health risks or environmental hazards. Proper characterization techniques, such as NMR and mass spectrometry, are essential for confirming its identity and purity in research and industrial applications.

Formula: C₁₀H₉ClO

InChI: InChI=1S/C10H9ClO/c11-10-4-2-1-3-9(10)7-5-8(12)6-7/h1-4,7H,5-6H2

InChI key: InChIKey=PZRHYHKZMBRCKP-UHFFFAOYSA-N

SMILES: ClC1=C(C=CC=C1)C2CC(=O)C2

Synonyms:

• 3-(2-Chlorophenyl)cyclobutanone
• Cyclobutanone, 3-(2-chlorophenyl)-

3-(2-Chlorophenyl)cyclobutan-1-one

CAS: 1080636-35-6

Formula: C₁₀H₉ClO

Molecular weight: 180.6309

Ref: IN-DA00HB2E

3-(2-Chlorophenyl)cyclobutanone

CAS: 1080636-35-6

3-(2-Chlorophenyl)cyclobutanone

Purity: ≥95%

Molecular weight: 180.63g/mol

Ref: 54-OR471197

3-(2-Chlorophenyl)cyclobutan-1-one

CAS: 1080636-35-6

The mechanism of the cyclobutanone cleavage reaction is a sequential intramolecular process in which the first step is a cyclobutanol intermediate that undergoes an expansion to form a six-membered ring with two unsaturated bonds. The second step involves bond cleavage and is triggered by the presence of palladium. This sequence can be used to synthesize 3-(2-chlorophenyl)cyclobutan-1-one.

Formula: C₁₀H₉ClO

Purity: Min. 95%

Molecular weight: 180.63 g/mol

Ref: 3D-FTB63635