(3,4-Dichlorophenyl)(hydroxy)acetic acid, with the CAS number 56071-99-9, is an organic compound characterized by the presence of a dichlorophenyl group and a hydroxyacetic acid moiety. This compound typically exhibits a white to off-white crystalline appearance and is soluble in polar solvents due to the presence of the hydroxy group, which enhances its hydrophilicity. The dichlorophenyl substituent contributes to its potential biological activity, as halogenated aromatic compounds often exhibit unique pharmacological properties. The compound may participate in various chemical reactions, including esterification and acylation, due to the carboxylic acid functional group. Its structural features suggest potential applications in pharmaceuticals or agrochemicals, where it may act as an intermediate or active ingredient. Additionally, the presence of chlorine atoms can influence its reactivity and interaction with biological systems, making it a subject of interest in medicinal chemistry and environmental studies. Safety and handling precautions should be observed, as with many organic compounds, to mitigate any potential hazards associated with exposure.

(3,4-dichlorophenyl)(hydroxy)acetic acid

56071-99-9: (3,4-Dichlorophenyl)(hydroxy)acetic acid, with the CAS number 56071-99-9, is an organic compound characterized by the presence of a dichlorophenyl group and a hydroxyacetic acid moiety. This compound typically exhibits a white to off-white crystalline appearance and is soluble in polar solvents due to the presence of the hydroxy group, which enhances its hydrophilicity. The dichlorophenyl substituent contributes to its potential biological activity, as halogenated aromatic compounds often exhibit unique pharmacological properties. The compound may participate in various chemical reactions, including esterification and acylation, due to the carboxylic acid functional group. Its structural features suggest potential applications in pharmaceuticals or agrochemicals, where it may act as an intermediate or active ingredient. Additionally, the presence of chlorine atoms can influence its reactivity and interaction with biological systems, making it a subject of interest in medicinal chemistry and environmental studies. Safety and handling precautions should be observed, as with many organic compounds, to mitigate any potential hazards associated with exposure.

CAS 56071-99-9

(3,4-dichlorophenyl)(hydroxy)acetic acid

3,4-Dichloro-Mandelic Acid

Ref: 4Z-S-0366

2-(3,4-Dichlorophenyl)-2-hydroxyacetic acid

Ref: 3D-GCA07199