2-Amino-1-(2,5-dimethoxyphenyl)-1-propanone, with the CAS number 103565-48-6, is an organic compound characterized by its structural features, which include an amino group and a propanone moiety attached to a substituted phenyl ring. The presence of two methoxy groups on the phenyl ring contributes to its unique chemical properties, influencing its reactivity and solubility. This compound is typically classified as an aromatic ketone and may exhibit biological activity due to the amino functional group, which can participate in various chemical reactions, including nucleophilic substitutions. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals or as a precursor in organic synthesis. Additionally, the compound's stability and reactivity can be affected by the electronic effects of the methoxy substituents, which can modulate its interaction with other chemical species. Overall, 2-amino-1-(2,5-dimethoxyphenyl)-1-propanone is of interest for its potential applications in research and industry, particularly in the fields of organic synthesis and drug development.

2-AMINO-1-(2,5-DIMETHOXYPHENYL)-1-PROPANONE

103565-48-6: 2-Amino-1-(2,5-dimethoxyphenyl)-1-propanone, with the CAS number 103565-48-6, is an organic compound characterized by its structural features, which include an amino group and a propanone moiety attached to a substituted phenyl ring. The presence of two methoxy groups on the phenyl ring contributes to its unique chemical properties, influencing its reactivity and solubility. This compound is typically classified as an aromatic ketone and may exhibit biological activity due to the amino functional group, which can participate in various chemical reactions, including nucleophilic substitutions. Its molecular structure suggests potential applications in medicinal chemistry, particularly in the development of pharmaceuticals or as a precursor in organic synthesis. Additionally, the compound's stability and reactivity can be affected by the electronic effects of the methoxy substituents, which can modulate its interaction with other chemical species. Overall, 2-amino-1-(2,5-dimethoxyphenyl)-1-propanone is of interest for its potential applications in research and industry, particularly in the fields of organic synthesis and drug development.

CAS 103565-48-6

2-AMINO-1-(2,5-DIMETHOXYPHENYL)-1-PROPANONE

Methoxamine Impurity 6

Ref: 4Z-M-215007