Trans-3-Fluorocyclobutanamine is a chemical compound characterized by its cyclobutane ring structure, which features a fluorine atom and an amine group. The "trans" designation indicates that the fluorine and amine substituents are positioned on opposite sides of the cyclobutane ring, influencing its stereochemistry and potentially its reactivity. This compound is of interest in medicinal chemistry and organic synthesis due to the presence of the fluorine atom, which can enhance biological activity and lipophilicity. The amine group may participate in hydrogen bonding, affecting solubility and interaction with biological targets. Additionally, the unique ring strain associated with cyclobutane can lead to distinctive chemical behavior compared to acyclic amines. As with many fluorinated compounds, trans-3-Fluorocyclobutanamine may exhibit different physical and chemical properties, such as boiling point, melting point, and reactivity, compared to its non-fluorinated counterparts. Its applications may extend to pharmaceuticals, agrochemicals, and materials science, depending on its specific properties and reactivity patterns.

trans-3-Fluorocyclobutanamine

1260670-33-4: Trans-3-Fluorocyclobutanamine is a chemical compound characterized by its cyclobutane ring structure, which features a fluorine atom and an amine group. The "trans" designation indicates that the fluorine and amine substituents are positioned on opposite sides of the cyclobutane ring, influencing its stereochemistry and potentially its reactivity. This compound is of interest in medicinal chemistry and organic synthesis due to the presence of the fluorine atom, which can enhance biological activity and lipophilicity. The amine group may participate in hydrogen bonding, affecting solubility and interaction with biological targets. Additionally, the unique ring strain associated with cyclobutane can lead to distinctive chemical behavior compared to acyclic amines. As with many fluorinated compounds, trans-3-Fluorocyclobutanamine may exhibit different physical and chemical properties, such as boiling point, melting point, and reactivity, compared to its non-fluorinated counterparts. Its applications may extend to pharmaceuticals, agrochemicals, and materials science, depending on its specific properties and reactivity patterns.

CAS 1260670-33-4

trans-3-Fluorocyclobutanamine

trans-3-Fluorocyclobutanamine

Ref: 54-PC105478