CAS 67688-28-2
:4-Phenylcycloheptanone
Description:
4-Phenylcycloheptanone is an organic compound characterized by its cycloheptanone structure, which features a seven-membered carbon ring with a ketone functional group and a phenyl substituent at the fourth position. This compound typically appears as a colorless to pale yellow liquid or solid, depending on the temperature and purity. It has a relatively high boiling point due to the presence of the ketone group, which contributes to its polar characteristics. The compound is known for its potential applications in organic synthesis and as an intermediate in the production of various pharmaceuticals and fine chemicals. Its reactivity is influenced by the ketone functional group, making it susceptible to nucleophilic attacks and other chemical transformations. Additionally, 4-Phenylcycloheptanone may exhibit interesting physical properties, such as solubility in organic solvents, which can vary based on the solvent's polarity. Safety data should be consulted for handling and storage, as with any chemical substance, to ensure proper precautions are taken.
Formula:C13H16O
InChI:InChI=1S/C13H16O/c14-13-8-4-7-12(9-10-13)11-5-2-1-3-6-11/h1-3,5-6,12H,4,7-10H2
InChI key:InChIKey=BVWZAWYJLYZIQD-UHFFFAOYSA-N
SMILES:O=C1CCC(CCC1)C2=CC=CC=C2
Synonyms:- 4-Phenylcycloheptanone
- Cycloheptanone, 4-phenyl-
- 4-Phenyl-cycloheptanone
- 4-phenylcycloheptan-1-one
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Found 1 products.
4-Phenylcycloheptan-1-one
CAS:<p>4-Phenylcycloheptan-1-one is a chemical compound that has been shown to have affinity for the piperidine receptor site in rat brain, which may be due to its structural similarity to piperidine. This chemical is a cyclohexanone derivative and is used as a medicinal agent. 4-Phenylcycloheptan-1-one has been shown to be an effective catalyst in asymmetric syntheses of cyclohexanones and other compounds, including catalytic asymmetric syntheses of phenylcycloheptanes.</p>Formula:C13H16OPurity:Min. 95%Molecular weight:188.26 g/mol
