3-(Furan-2-yl)propan-1-amine, with the CAS number 4428-38-0, is an organic compound characterized by its furan ring, which is a five-membered aromatic heterocycle containing oxygen. This compound features a propan-1-amine chain, indicating the presence of an amine functional group (-NH2) attached to a three-carbon alkyl chain. The furan moiety contributes to its aromatic properties and can influence its reactivity and interactions with other molecules. Typically, compounds like this may exhibit biological activity, making them of interest in medicinal chemistry and drug development. The presence of both the furan and amine groups suggests potential for hydrogen bonding and other intermolecular interactions, which can affect solubility and stability. Additionally, the compound may be synthesized through various organic reactions, including amination processes. Its physical properties, such as melting point, boiling point, and solubility, would depend on the specific molecular interactions and the environment in which it is studied. Overall, 3-(furan-2-yl)propan-1-amine is a versatile compound with potential applications in various fields of chemistry and pharmacology.

3-(furan-2-yl)propan-1-amine

4428-38-0: 3-(Furan-2-yl)propan-1-amine, with the CAS number 4428-38-0, is an organic compound characterized by its furan ring, which is a five-membered aromatic heterocycle containing oxygen. This compound features a propan-1-amine chain, indicating the presence of an amine functional group (-NH2) attached to a three-carbon alkyl chain. The furan moiety contributes to its aromatic properties and can influence its reactivity and interactions with other molecules. Typically, compounds like this may exhibit biological activity, making them of interest in medicinal chemistry and drug development. The presence of both the furan and amine groups suggests potential for hydrogen bonding and other intermolecular interactions, which can affect solubility and stability. Additionally, the compound may be synthesized through various organic reactions, including amination processes. Its physical properties, such as melting point, boiling point, and solubility, would depend on the specific molecular interactions and the environment in which it is studied. Overall, 3-(furan-2-yl)propan-1-amine is a versatile compound with potential applications in various fields of chemistry and pharmacology.

CAS 4428-38-0

3-(furan-2-yl)propan-1-amine

3-(2-furyl)propan-1-amine oxalate

Ref: IN-DA00DCQ5

3-(2-furyl)-1-propanamine

Ref: 10-F311082