4-Ethylcyclohexene is a cyclic hydrocarbon with the molecular formula C10H16, characterized by a cyclohexene ring substituted with an ethyl group at the 4-position. This compound is a colorless to pale yellow liquid at room temperature and possesses a distinctive, sweet, and somewhat floral odor. It is classified as an alkene due to the presence of a double bond within the cyclohexene structure, which contributes to its reactivity, particularly in addition reactions. 4-Ethylcyclohexene is relatively insoluble in water but soluble in organic solvents such as ethanol and ether. It is primarily used in organic synthesis and as an intermediate in the production of various chemicals. Safety considerations include flammability and potential skin and eye irritation, necessitating appropriate handling and storage measures. Overall, 4-ethylcyclohexene serves as an important compound in the field of organic chemistry, particularly in the synthesis of more complex molecules.

4-ethylcyclohexene

3742-42-5: 4-Ethylcyclohexene is a cyclic hydrocarbon with the molecular formula C10H16, characterized by a cyclohexene ring substituted with an ethyl group at the 4-position. This compound is a colorless to pale yellow liquid at room temperature and possesses a distinctive, sweet, and somewhat floral odor. It is classified as an alkene due to the presence of a double bond within the cyclohexene structure, which contributes to its reactivity, particularly in addition reactions. 4-Ethylcyclohexene is relatively insoluble in water but soluble in organic solvents such as ethanol and ether. It is primarily used in organic synthesis and as an intermediate in the production of various chemicals. Safety considerations include flammability and potential skin and eye irritation, necessitating appropriate handling and storage measures. Overall, 4-ethylcyclohexene serves as an important compound in the field of organic chemistry, particularly in the synthesis of more complex molecules.

<p>4-Ethylcyclohexene is a compound that is used as an intermediate in the manufacture of chemicals. It is obtained by ring-opening of the cyclohexene molecule with the addition of halides. The reaction proceeds with high yields and selectivity when using homogeneous catalysts such as ruthenium, which are able to catalyze both the ring-opening and the subsequent halide addition reactions. The transformation of 4-ethylcyclohexene to 4-propylcyclohexene can be carried out using protonation or nitrate. The conversion from 4-propylcyclohexene to 4-butylcyclohexene can be accomplished by oxidation with oxygen or peroxide, followed by hydrogenation, or by gas chromatography/mass spectrometry.</p>

CAS 3742-42-5

4-ethylcyclohexene

4-Ethylcyclohexene

Ref: 3D-FE152357