3-(Phenylamino)propan-1-ol, also known by its CAS number 31121-11-6, is an organic compound characterized by the presence of both an amino group and an alcohol functional group. Structurally, it features a propanol backbone with a phenylamino substituent, which contributes to its unique chemical properties. This compound is typically a colorless to pale yellow liquid or solid, depending on its purity and form. It is soluble in polar solvents due to the hydroxyl group, which can engage in hydrogen bonding, enhancing its reactivity and potential applications in organic synthesis. The amino group can participate in various reactions, including nucleophilic substitutions and coupling reactions, making it valuable in the synthesis of pharmaceuticals and agrochemicals. Additionally, the presence of the phenyl group can influence the compound's electronic properties and stability. Overall, 3-(phenylamino)propan-1-ol is a versatile compound with potential applications in medicinal chemistry and materials science.

3-(phenylamino)propan-1-ol

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3-Anilino-1-propanol

3-Anilino-1-propanol is a chemical compound that contains one hydroxyl group and three aniline rings. 3-Anilino-1-propanol is synthesized by the reaction of ethylene with aniline in the presence of nitrobenzene and chloride. The reaction system is made up of three steps: electron transfer, nucleophilic attack, and proton transfer. The functional theory has been used to rationalize the mechanism of this reaction system. Kinetic studies have shown that chloride plays a crucial role in the reaction mechanism, which may be due to its ability to stabilize the intermediate chloroethanol molecule.

CAS 31121-11-6: 3-(phenylamino)propan-1-ol

3-Anilino-1-propanol

Ref: 3B-A2248

3-Anilino-1-propanol

Ref: 3D-FA174975

3-Anilino-1-propanol

Ref: 54-OR938169

1-Propanol, 3-(phenylamino)-

Ref: IN-DA00325P