CAS 41564-62-9

1-Penten-3-one, 1-(4-chlorophenyl)-4,4-dimethyl-, (E)-

Description:

1-Penten-3-one, 1-(4-chlorophenyl)-4,4-dimethyl-, (E)-, with the CAS number 41564-62-9, is an organic compound characterized by its unique structure that includes a pentenone backbone and a substituted aromatic ring. This compound features a double bond between the first and second carbon atoms, contributing to its reactivity and potential applications in organic synthesis. The presence of the 4-chlorophenyl group enhances its aromatic properties and may influence its biological activity. The (E)- configuration indicates that the substituents around the double bond are on opposite sides, which can affect the compound's physical and chemical properties, such as boiling point and solubility. Generally, compounds of this nature may exhibit interesting properties such as volatility and reactivity, making them useful in various chemical reactions, including those in pharmaceuticals and agrochemicals. Additionally, the presence of chlorine in the structure can impart specific characteristics, such as increased lipophilicity or altered interaction with biological targets.

Formula: C₁₃H₁₅ClO

(1E)-1-(4-Chlorophenyl)-4,4-dimethyl-1-penten-3-one-D9

Controlled Product

CAS: 41564-62-9

Applications (1E)-1-(4-Chlorophenyl)-4,4-dimethyl-1-penten-3-one-D9 is an intermediate in the synthesis of Isotope labelled Tebuconazole (T013002), which is an ergosterol biosynthesis inhibitor present in most pesticide formulations (1,2). Various uptake is observed in plants (3). Drinking water Contaminant Candidate List 3 - CCL 3 as per United States Environmental Protection Agency (EPA). Environmental contaminants; Food contaminants.

Formula: C₁₃D₉H₆ClO

Color and Shape: Neat

Molecular weight: 231.766

Ref: TR-C992565