Ethanedione, specifically the compound with the name (2,4-dimethoxyphenyl)(2-hydroxy-4,6-dimethoxyphenyl)-, is a chemical substance characterized by its complex structure featuring two aromatic rings substituted with methoxy and hydroxyl groups. This compound is part of a larger class of organic molecules known for their potential applications in pharmaceuticals and organic synthesis. The presence of multiple methoxy groups enhances its solubility in organic solvents and may influence its reactivity and interaction with biological systems. The hydroxyl group contributes to its potential as a hydrogen bond donor, which can affect its chemical behavior and interactions. The compound's molecular structure suggests it may exhibit interesting optical properties, making it a candidate for studies in materials science or medicinal chemistry. Additionally, the specific arrangement of substituents can lead to unique electronic properties, which may be exploited in various applications, including dye synthesis or as intermediates in organic reactions. Overall, this compound exemplifies the diversity and complexity of organic chemistry.

Ethanedione, (2,4-dimethoxyphenyl)(2-hydroxy-4,6-dimethoxyphenyl)-

88092-57-3: Ethanedione, specifically the compound with the name (2,4-dimethoxyphenyl)(2-hydroxy-4,6-dimethoxyphenyl)-, is a chemical substance characterized by its complex structure featuring two aromatic rings substituted with methoxy and hydroxyl groups. This compound is part of a larger class of organic molecules known for their potential applications in pharmaceuticals and organic synthesis. The presence of multiple methoxy groups enhances its solubility in organic solvents and may influence its reactivity and interaction with biological systems. The hydroxyl group contributes to its potential as a hydrogen bond donor, which can affect its chemical behavior and interactions. The compound's molecular structure suggests it may exhibit interesting optical properties, making it a candidate for studies in materials science or medicinal chemistry. Additionally, the specific arrangement of substituents can lead to unique electronic properties, which may be exploited in various applications, including dye synthesis or as intermediates in organic reactions. Overall, this compound exemplifies the diversity and complexity of organic chemistry.

CAS 88092-57-3

Ethanedione, (2,4-dimethoxyphenyl)(2-hydroxy-4,6-dimethoxyphenyl)-

Ethanedione, (2,4-dimethoxyphenyl)(2-hydroxy-4,6-dimethoxyphenyl)-

Ref: IN-DA004EJH