3-Phenyloxetane, with the CAS number 10317-13-2, is a cyclic ether characterized by a three-membered oxetane ring substituted with a phenyl group. This compound exhibits a unique combination of properties due to the presence of both the aromatic phenyl group and the strained oxetane ring. Typically, 3-phenyloxetane is a colorless liquid at room temperature, with a relatively low boiling point compared to larger cyclic ethers. Its structure contributes to its reactivity, making it a potential candidate for various chemical reactions, including ring-opening polymerization and electrophilic aromatic substitution. The presence of the phenyl group enhances its stability and solubility in organic solvents, while also influencing its chemical behavior. 3-Phenyloxetane can be utilized in organic synthesis and may serve as an intermediate in the production of more complex molecules. Safety data indicates that, like many organic compounds, it should be handled with care, as it may pose risks such as flammability or irritation upon contact.

3-phenyloxetane

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3-Phenyloxetane

3-Phenyloxetane is an organic compound that belongs to the class of oxetanes. It is a nucleophilic, hydrophobic molecule with a ring-opening reaction mechanism. 3-Phenyloxetane reacts with amines to form trifluoroacetamide derivatives, which are catalyzed by trifluoromethanesulfonic acid. 3-Phenyloxetane also has inhibitory potency against nitro compounds and epoxides, as well as styrene.

CAS 10317-13-2: 3-phenyloxetane

3-Phenyloxetane

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3-Phenyloxetane

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3-Phenyloxetane

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3-Phenyloxetane

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