3-(2-Chlorophenoxy)propan-1-amine, with the CAS number 50911-59-6, is an organic compound characterized by its amine functional group and a chlorophenoxy substituent. This compound features a propan-1-amine backbone, which is a three-carbon chain terminating in an amine group (-NH2), and a 2-chlorophenoxy group, indicating the presence of a chlorinated phenyl ring attached via an ether linkage. The chlorophenyl moiety contributes to the compound's potential biological activity and hydrophobic characteristics. Typically, compounds of this nature may exhibit moderate solubility in organic solvents and limited solubility in water due to the presence of both hydrophilic (amine) and hydrophobic (phenyl) components. The presence of the chlorine atom can influence the compound's reactivity and interaction with biological systems, potentially affecting its pharmacological properties. As with many amines, it may participate in hydrogen bonding, influencing its physical properties and reactivity in various chemical environments. Safety and handling precautions should be observed, as with all chemical substances, particularly those with potential biological activity.

3-(2-chlorophenoxy)propan-1-amine

50911-59-6: 3-(2-Chlorophenoxy)propan-1-amine, with the CAS number 50911-59-6, is an organic compound characterized by its amine functional group and a chlorophenoxy substituent. This compound features a propan-1-amine backbone, which is a three-carbon chain terminating in an amine group (-NH2), and a 2-chlorophenoxy group, indicating the presence of a chlorinated phenyl ring attached via an ether linkage. The chlorophenyl moiety contributes to the compound's potential biological activity and hydrophobic characteristics. Typically, compounds of this nature may exhibit moderate solubility in organic solvents and limited solubility in water due to the presence of both hydrophilic (amine) and hydrophobic (phenyl) components. The presence of the chlorine atom can influence the compound's reactivity and interaction with biological systems, potentially affecting its pharmacological properties. As with many amines, it may participate in hydrogen bonding, influencing its physical properties and reactivity in various chemical environments. Safety and handling precautions should be observed, as with all chemical substances, particularly those with potential biological activity.

CAS 50911-59-6

3-(2-chlorophenoxy)propan-1-amine

3-(2-Chlorophenoxy)propan-1-amine

Ref: IN-DA00DBU5

3-(2-Chlorophenoxy)propylamine

Ref: 54-OR953830