Ethylmetrienone, with the CAS number 848-04-4, is a synthetic organic compound that belongs to the class of ketones. It is characterized by its unique structure, which includes a conjugated system that contributes to its chemical reactivity and potential applications. Ethylmetrienone typically exhibits a yellow to brown color in its pure form and is known for its distinctive odor. The compound is soluble in organic solvents, making it useful in various chemical reactions and formulations. Ethylmetrienone has garnered interest in the fields of organic synthesis and medicinal chemistry due to its potential biological activities, including antimicrobial and anti-inflammatory properties. However, like many synthetic compounds, it should be handled with care, as it may pose health risks if ingested or inhaled. Proper safety protocols should be followed when working with this substance in laboratory settings. Overall, ethylmetrienone represents a versatile compound with applications in research and industry, although further studies are necessary to fully understand its properties and potential uses.

Ethylmetrienone

848-04-4: 18-Methylestrone methyl ether, 13-Ethyl-3-methoxygona-1,3,5(10)-trien-17-one

Levonorgestrel Impurity 4 (Ethylmetrienone)

Ethylmetrienone is an ether that is prepared by a Wittig reaction between methylchlorosilane and ethylene oxide. The wittig reaction is a condensation reaction, which can be used to make methyl esters from carboxylic acids. This compound is also an epimer of desogestrel, which can be converted back to the original chemical by the intramolecular rearrangement of the cyclopropene ring. Ethylmetrienone has been shown to be assembled with phosphonium salts to form phosphonium salts and then undergo an acid-catalyzed isomerization in order to form a new compound.

CAS 848-04-4: Ethylmetrienone

Levonorgestrel Impurity 4 (Ethylmetrienone)

Ref: 4Z-L-2232

Ethylmetrienone

Ref: 3D-AAA84804