4-Methoxy-N-(prop-2-en-1-yl)aniline, with the CAS number 71954-46-6, is an organic compound characterized by its aniline structure, which features an amino group (-NH2) attached to a benzene ring. The presence of a methoxy group (-OCH3) at the para position relative to the amino group enhances its electron-donating properties, influencing its reactivity and solubility. The alkenyl substituent, prop-2-en-1-yl, introduces a double bond, which can participate in various chemical reactions, including polymerization and electrophilic addition. This compound is likely to exhibit moderate polarity due to the combination of hydrophobic aromatic and hydrophilic functional groups, affecting its solubility in organic solvents and water. Additionally, it may display biological activity, making it of interest in medicinal chemistry and materials science. Its synthesis typically involves the alkylation of an aniline derivative, and it may be used as an intermediate in the production of dyes, pharmaceuticals, or agrochemicals. Safety data should be consulted for handling and potential hazards associated with this compound.

4-methoxy-N-(prop-2-en-1-yl)aniline

71954-46-6: 4-Methoxy-N-(prop-2-en-1-yl)aniline, with the CAS number 71954-46-6, is an organic compound characterized by its aniline structure, which features an amino group (-NH2) attached to a benzene ring. The presence of a methoxy group (-OCH3) at the para position relative to the amino group enhances its electron-donating properties, influencing its reactivity and solubility. The alkenyl substituent, prop-2-en-1-yl, introduces a double bond, which can participate in various chemical reactions, including polymerization and electrophilic addition. This compound is likely to exhibit moderate polarity due to the combination of hydrophobic aromatic and hydrophilic functional groups, affecting its solubility in organic solvents and water. Additionally, it may display biological activity, making it of interest in medicinal chemistry and materials science. Its synthesis typically involves the alkylation of an aniline derivative, and it may be used as an intermediate in the production of dyes, pharmaceuticals, or agrochemicals. Safety data should be consulted for handling and potential hazards associated with this compound.

CAS 71954-46-6

4-methoxy-N-(prop-2-en-1-yl)aniline

Allyl-(4-methoxy-phenyl)-amine

Ref: 54-OR97344

Allyl-(4-methoxy-phenyl)-amine

Ref: 10-F475623