1-(Tetrahydrofuran-2-yl)-N-(thiophen-3-ylmethyl)methanamine, identified by its CAS number 892592-66-4, is a chemical compound characterized by its unique structural features. It contains a tetrahydrofuran ring, which is a five-membered cyclic ether known for its polar aprotic properties, enhancing solubility in various organic solvents. The presence of a thiophene moiety, a five-membered aromatic ring containing sulfur, contributes to the compound's potential electronic properties and reactivity. This compound is likely to exhibit moderate to high lipophilicity due to the hydrophobic nature of the thiophene and the tetrahydrofuran ring, which may influence its biological activity and interaction with biological membranes. Additionally, the amine functional group suggests potential for hydrogen bonding, which can affect its solubility and reactivity. Overall, this compound may have applications in medicinal chemistry, particularly in the development of pharmaceuticals, owing to its structural diversity and potential biological activity. However, specific properties such as melting point, boiling point, and reactivity would require empirical data for precise characterization.

1-(tetrahydrofuran-2-yl)-N-(thiophen-3-ylmethyl)methanamine

892592-66-4: 1-(Tetrahydrofuran-2-yl)-N-(thiophen-3-ylmethyl)methanamine, identified by its CAS number 892592-66-4, is a chemical compound characterized by its unique structural features. It contains a tetrahydrofuran ring, which is a five-membered cyclic ether known for its polar aprotic properties, enhancing solubility in various organic solvents. The presence of a thiophene moiety, a five-membered aromatic ring containing sulfur, contributes to the compound's potential electronic properties and reactivity. This compound is likely to exhibit moderate to high lipophilicity due to the hydrophobic nature of the thiophene and the tetrahydrofuran ring, which may influence its biological activity and interaction with biological membranes. Additionally, the amine functional group suggests potential for hydrogen bonding, which can affect its solubility and reactivity. Overall, this compound may have applications in medicinal chemistry, particularly in the development of pharmaceuticals, owing to its structural diversity and potential biological activity. However, specific properties such as melting point, boiling point, and reactivity would require empirical data for precise characterization.

CAS 892592-66-4

1-(tetrahydrofuran-2-yl)-N-(thiophen-3-ylmethyl)methanamine

1-(Tetrahydrofuran-2-yl)-N-(thiophen-3-ylmethyl)methanamine

Ref: IN-DA0041Z1