1-(4-Ethoxy-2-hydroxyphenyl)ethanone, with the CAS number 37470-42-1, is an organic compound characterized by its phenolic structure and ketone functional group. It features an ethoxy group and a hydroxy group attached to a phenyl ring, which contributes to its potential reactivity and solubility properties. The presence of the hydroxy group suggests that it may exhibit hydrogen bonding capabilities, influencing its solubility in polar solvents. This compound is likely to be a solid at room temperature, with a specific melting point and boiling point that would depend on its molecular interactions. It may also exhibit moderate to high stability under standard conditions, although it could be sensitive to light or heat, which is common for many organic compounds. Its chemical properties may allow it to participate in various reactions, such as electrophilic aromatic substitution or oxidation, making it of interest in synthetic organic chemistry and potentially in pharmaceutical applications. Further studies would be necessary to fully elucidate its biological activity and practical applications.

1-(4-ethoxy-2-hydroxyphenyl)ethanone

37470-42-1: 1-(4-Ethoxy-2-hydroxyphenyl)ethanone, with the CAS number 37470-42-1, is an organic compound characterized by its phenolic structure and ketone functional group. It features an ethoxy group and a hydroxy group attached to a phenyl ring, which contributes to its potential reactivity and solubility properties. The presence of the hydroxy group suggests that it may exhibit hydrogen bonding capabilities, influencing its solubility in polar solvents. This compound is likely to be a solid at room temperature, with a specific melting point and boiling point that would depend on its molecular interactions. It may also exhibit moderate to high stability under standard conditions, although it could be sensitive to light or heat, which is common for many organic compounds. Its chemical properties may allow it to participate in various reactions, such as electrophilic aromatic substitution or oxidation, making it of interest in synthetic organic chemistry and potentially in pharmaceutical applications. Further studies would be necessary to fully elucidate its biological activity and practical applications.

CAS 37470-42-1

1-(4-ethoxy-2-hydroxyphenyl)ethanone

1-(4-Ethoxy-2-hydroxyphenyl)ethan-1-one

Ref: 10-F730305

4′-Ethoxy-2′-hydroxyacetophenone

Ref: IN-DA003KLQ