2-Amino-1-(3,5-dichlorophenyl)ethanol, with the CAS number 78982-78-2, is an organic compound characterized by the presence of an amino group and a hydroxyl group attached to a two-carbon ethyl chain, along with a dichlorophenyl substituent. This compound typically appears as a solid or crystalline substance and is soluble in polar solvents due to the hydroxyl group, which can engage in hydrogen bonding. The dichlorophenyl moiety contributes to its hydrophobic characteristics and may influence its biological activity. The presence of chlorine atoms on the phenyl ring can enhance the compound's reactivity and lipophilicity, potentially affecting its pharmacological properties. 2-Amino-1-(3,5-dichlorophenyl)ethanol may be of interest in medicinal chemistry, particularly in the development of pharmaceuticals, due to its structural features that can interact with biological targets. As with many amines and alcohols, it may exhibit basic properties and can participate in various chemical reactions, including nucleophilic substitutions and condensation reactions.

2-amino-1-(3,5-dichlorophenyl)ethanol

78982-78-2: 2-Amino-1-(3,5-dichlorophenyl)ethanol, with the CAS number 78982-78-2, is an organic compound characterized by the presence of an amino group and a hydroxyl group attached to a two-carbon ethyl chain, along with a dichlorophenyl substituent. This compound typically appears as a solid or crystalline substance and is soluble in polar solvents due to the hydroxyl group, which can engage in hydrogen bonding. The dichlorophenyl moiety contributes to its hydrophobic characteristics and may influence its biological activity. The presence of chlorine atoms on the phenyl ring can enhance the compound's reactivity and lipophilicity, potentially affecting its pharmacological properties. 2-Amino-1-(3,5-dichlorophenyl)ethanol may be of interest in medicinal chemistry, particularly in the development of pharmaceuticals, due to its structural features that can interact with biological targets. As with many amines and alcohols, it may exhibit basic properties and can participate in various chemical reactions, including nucleophilic substitutions and condensation reactions.

CAS 78982-78-2

2-amino-1-(3,5-dichlorophenyl)ethanol

2-Amino-1-(3,5-dichlorophenyl)ethan-1-ol

Ref: 3D-DDA98278