3-(3-Methylphenyl)-1-(4-methylphenyl)prop-2-en-1-one, commonly referred to as a type of chalcone, is an organic compound characterized by its structure, which features a prop-2-en-1-one backbone with two aromatic rings substituted at specific positions. This compound typically exhibits a yellow to orange color and is known for its potential biological activities, including antioxidant, anti-inflammatory, and antimicrobial properties. Chalcones, including this compound, often serve as intermediates in the synthesis of various pharmaceuticals and agrochemicals. The presence of methyl groups on the phenyl rings can influence the compound's solubility and reactivity, making it of interest in both synthetic and medicinal chemistry. Additionally, its conjugated double bond system contributes to its UV-Vis absorption properties, which can be utilized in various applications, including dye production and photochemical studies. As with many organic compounds, safety and handling precautions should be observed due to potential toxicity or reactivity.

3-(3-methylphenyl)-1-(4-methylphenyl)prop-2-en-1-one

52182-33-9: 3-(3-Methylphenyl)-1-(4-methylphenyl)prop-2-en-1-one, commonly referred to as a type of chalcone, is an organic compound characterized by its structure, which features a prop-2-en-1-one backbone with two aromatic rings substituted at specific positions. This compound typically exhibits a yellow to orange color and is known for its potential biological activities, including antioxidant, anti-inflammatory, and antimicrobial properties. Chalcones, including this compound, often serve as intermediates in the synthesis of various pharmaceuticals and agrochemicals. The presence of methyl groups on the phenyl rings can influence the compound's solubility and reactivity, making it of interest in both synthetic and medicinal chemistry. Additionally, its conjugated double bond system contributes to its UV-Vis absorption properties, which can be utilized in various applications, including dye production and photochemical studies. As with many organic compounds, safety and handling precautions should be observed due to potential toxicity or reactivity.

CAS 52182-33-9

3-(3-methylphenyl)-1-(4-methylphenyl)prop-2-en-1-one

(2E)-3-(3-methylphenyl)-1-(4-methylphenyl)prop-2-en-1-one

Ref: 10-F523986