3,4-Diaminobenzeneethanol, also known as 3,4-diaminophenylethanol, is an organic compound characterized by the presence of two amino groups (-NH2) and a hydroxyl group (-OH) attached to a benzene ring. This compound features a phenolic structure, which contributes to its reactivity and potential applications in various chemical processes. The amino groups can participate in hydrogen bonding and nucleophilic reactions, making it useful in the synthesis of dyes, pharmaceuticals, and polymers. The hydroxyl group enhances its solubility in polar solvents and can also engage in hydrogen bonding, influencing its physical properties. 3,4-Diaminobenzeneethanol is typically a solid at room temperature and may exhibit moderate toxicity, necessitating careful handling. Its chemical behavior is influenced by the electron-donating nature of the amino groups, which can affect the compound's reactivity and interaction with other chemical species. Overall, this compound is of interest in both academic research and industrial applications due to its versatile functional groups.

3,4-Diaminobenzeneethanol

15788-14-4: 3,4-Diaminobenzeneethanol, also known as 3,4-diaminophenylethanol, is an organic compound characterized by the presence of two amino groups (-NH2) and a hydroxyl group (-OH) attached to a benzene ring. This compound features a phenolic structure, which contributes to its reactivity and potential applications in various chemical processes. The amino groups can participate in hydrogen bonding and nucleophilic reactions, making it useful in the synthesis of dyes, pharmaceuticals, and polymers. The hydroxyl group enhances its solubility in polar solvents and can also engage in hydrogen bonding, influencing its physical properties. 3,4-Diaminobenzeneethanol is typically a solid at room temperature and may exhibit moderate toxicity, necessitating careful handling. Its chemical behavior is influenced by the electron-donating nature of the amino groups, which can affect the compound's reactivity and interaction with other chemical species. Overall, this compound is of interest in both academic research and industrial applications due to its versatile functional groups.

CAS 15788-14-4

3,4-Diaminobenzeneethanol

2-(3,4-Diaminophenyl)ethanol

Ref: IN-DA001PSX

2-(3,4-Diaminophenyl)ethan-1-ol

Ref: 3D-QAA78814