1-(3,4-Dihydroxyphenyl)-1,2-diaminoethane, also known as a derivative of catecholamine, is an organic compound characterized by the presence of two amino groups and a catechol moiety. This compound features a benzene ring with two hydroxyl groups positioned at the 3 and 4 positions, contributing to its phenolic properties. The amino groups are attached to a two-carbon ethane chain, which enhances its potential for biological activity. This structure allows for hydrogen bonding and interactions with various biological targets, making it of interest in medicinal chemistry. The compound is typically soluble in polar solvents due to its functional groups, and it may exhibit antioxidant properties owing to the presence of the catechol structure. Its reactivity can be influenced by the amino and hydroxyl groups, which can participate in various chemical reactions, including oxidation and complexation. Overall, this compound's unique structural features suggest potential applications in pharmaceuticals and biochemistry, particularly in the study of neurotransmitter systems and related pathways.

1-(3,4-dihydroxyphenyl)-1,2-diaminoethane

132261-26-8: 1-(3,4-Dihydroxyphenyl)-1,2-diaminoethane, also known as a derivative of catecholamine, is an organic compound characterized by the presence of two amino groups and a catechol moiety. This compound features a benzene ring with two hydroxyl groups positioned at the 3 and 4 positions, contributing to its phenolic properties. The amino groups are attached to a two-carbon ethane chain, which enhances its potential for biological activity. This structure allows for hydrogen bonding and interactions with various biological targets, making it of interest in medicinal chemistry. The compound is typically soluble in polar solvents due to its functional groups, and it may exhibit antioxidant properties owing to the presence of the catechol structure. Its reactivity can be influenced by the amino and hydroxyl groups, which can participate in various chemical reactions, including oxidation and complexation. Overall, this compound's unique structural features suggest potential applications in pharmaceuticals and biochemistry, particularly in the study of neurotransmitter systems and related pathways.

CAS 132261-26-8

1-(3,4-dihydroxyphenyl)-1,2-diaminoethane

1,2-Benzenediol, 4-(1,2-diaminoethyl)-

Ref: IN-DA0010GK