CAS 152714-07-3
:Cyclobutanone, 3-(4-chlorophenyl)-
Description:
Cyclobutanone, 3-(4-chlorophenyl)- is an organic compound characterized by a cyclobutanone ring substituted with a para-chlorophenyl group. This compound features a four-membered cyclic ketone structure, which contributes to its unique chemical properties. The presence of the chlorophenyl group enhances its reactivity and influences its physical properties, such as solubility and boiling point. Cyclobutanones generally exhibit a degree of strain due to the small ring size, which can affect their stability and reactivity in chemical reactions. The para-chloro substitution introduces an electron-withdrawing effect, potentially impacting the compound's reactivity in electrophilic aromatic substitution reactions. This compound may be of interest in various fields, including medicinal chemistry and materials science, due to its potential applications in synthesizing more complex molecules. As with many organic compounds, safety precautions should be taken when handling cyclobutanone derivatives, as they may pose health risks or environmental hazards.
Formula:C10H9ClO
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Found 4 products.
3-(4-Chlorophenyl)Cyclobutanone
CAS:Formula:C10H9ClOPurity:97%Color and Shape:LiquidMolecular weight:180.63093-(4-Chlorophenyl)-cyclobutane-1-one
CAS:<p>3-(4-Chlorophenyl)-cyclobutane-1-one</p>Purity:97%Molecular weight:180.63g/mol3-(4-chlorophenyl)cyclobutan-1-one
CAS:Formula:C10H9ClOPurity:98%Color and Shape:LiquidMolecular weight:180.633-(4-chlorophenyl)cyclobutanone
CAS:<p>Cyclobutanone is a cyclic ketone that is used as a reagent in organic synthesis. It can be converted to the corresponding oxime by treatment with hydroxylamine. The oxime then reacts with an ester to form the corresponding ester of cyclobutanone. Cyclobutanones are also used as coupling agents for amines, alcohols, and carboxylic acids.</p>Formula:C10H9ClOPurity:Min. 95%Molecular weight:180.63 g/mol
