1-(4-Bromophenyl)-ethane-1,2-diamine, with the CAS number 735208-91-0, is an organic compound characterized by its amine functional groups and a bromophenyl substituent. This compound features a two-carbon ethane backbone with amino groups (-NH2) attached to the first and second carbon atoms, and a bromine atom attached to a phenyl ring at the para position relative to the amine group. The presence of the bromine atom enhances its reactivity and may influence its biological activity, making it of interest in medicinal chemistry. The compound is likely to be a solid at room temperature, with potential applications in pharmaceuticals or as an intermediate in organic synthesis. Its solubility in various solvents can vary, typically being more soluble in polar solvents due to the presence of the amine groups. Additionally, the compound may exhibit basic properties due to the amine functionalities, allowing it to participate in various chemical reactions, including nucleophilic substitutions and coupling reactions. Safety and handling precautions should be observed due to the presence of bromine and amine groups, which can pose health risks.

1-(4-bromophenyl)-ethane-1,2-diamine

735208-91-0: 1-(4-Bromophenyl)-ethane-1,2-diamine, with the CAS number 735208-91-0, is an organic compound characterized by its amine functional groups and a bromophenyl substituent. This compound features a two-carbon ethane backbone with amino groups (-NH2) attached to the first and second carbon atoms, and a bromine atom attached to a phenyl ring at the para position relative to the amine group. The presence of the bromine atom enhances its reactivity and may influence its biological activity, making it of interest in medicinal chemistry. The compound is likely to be a solid at room temperature, with potential applications in pharmaceuticals or as an intermediate in organic synthesis. Its solubility in various solvents can vary, typically being more soluble in polar solvents due to the presence of the amine groups. Additionally, the compound may exhibit basic properties due to the amine functionalities, allowing it to participate in various chemical reactions, including nucleophilic substitutions and coupling reactions. Safety and handling precautions should be observed due to the presence of bromine and amine groups, which can pose health risks.

CAS 735208-91-0

1-(4-bromophenyl)-ethane-1,2-diamine