2-Aminoheptafluoronaphthalene, with the CAS number 1146-66-3, is a fluorinated aromatic compound characterized by the presence of an amino group and multiple fluorine atoms attached to a naphthalene ring structure. This compound exhibits unique properties due to the electronegative fluorine substituents, which can influence its reactivity, polarity, and solubility. The amino group introduces basicity and potential for hydrogen bonding, making it a candidate for various chemical reactions, including nucleophilic substitutions. The heptafluoro substitution pattern contributes to its hydrophobic nature and thermal stability, which can be advantageous in applications such as specialty coatings, pharmaceuticals, and materials science. Additionally, the presence of fluorine atoms often enhances the compound's resistance to chemical degradation and increases its performance in high-temperature environments. Overall, 2-aminoheptafluoronaphthalene is notable for its unique combination of properties derived from both its fluorinated structure and the amino functional group.

2-aminoheptafluoronaphthalene

1146-66-3: 2-Aminoheptafluoronaphthalene, with the CAS number 1146-66-3, is a fluorinated aromatic compound characterized by the presence of an amino group and multiple fluorine atoms attached to a naphthalene ring structure. This compound exhibits unique properties due to the electronegative fluorine substituents, which can influence its reactivity, polarity, and solubility. The amino group introduces basicity and potential for hydrogen bonding, making it a candidate for various chemical reactions, including nucleophilic substitutions. The heptafluoro substitution pattern contributes to its hydrophobic nature and thermal stability, which can be advantageous in applications such as specialty coatings, pharmaceuticals, and materials science. Additionally, the presence of fluorine atoms often enhances the compound's resistance to chemical degradation and increases its performance in high-temperature environments. Overall, 2-aminoheptafluoronaphthalene is notable for its unique combination of properties derived from both its fluorinated structure and the amino functional group.

CAS 1146-66-3

2-aminoheptafluoronaphthalene

2-Naphthalenamine, 1,3,4,5,6,7,8-heptafluoro-

Ref: IN-DA000ERX

2-Aminoheptafluoronaphthalene

Ref: 54-PC0974