1-Fluoro-2-aminonaphthalene is an organic compound characterized by the presence of both a fluorine atom and an amino group attached to a naphthalene ring system. This compound features a naphthalene backbone, which consists of two fused benzene rings, providing it with a stable aromatic structure. The fluorine substituent typically enhances the compound's reactivity and can influence its electronic properties, while the amino group contributes to its potential as a nucleophile. The presence of these functional groups suggests that 1-fluoro-2-aminonaphthalene may participate in various chemical reactions, including electrophilic aromatic substitution and nucleophilic reactions. Additionally, the compound may exhibit interesting physical properties, such as solubility in organic solvents and potential fluorescence, making it of interest in fields like materials science and organic synthesis. Its specific applications may vary, but compounds of this nature are often explored for their roles in pharmaceuticals, agrochemicals, and as intermediates in organic synthesis. Safety data should be consulted for handling and storage, as with any chemical substance.

1-fluoro-2-aminonaphthalene

14554-00-8: 1-Fluoro-2-aminonaphthalene is an organic compound characterized by the presence of both a fluorine atom and an amino group attached to a naphthalene ring system. This compound features a naphthalene backbone, which consists of two fused benzene rings, providing it with a stable aromatic structure. The fluorine substituent typically enhances the compound's reactivity and can influence its electronic properties, while the amino group contributes to its potential as a nucleophile. The presence of these functional groups suggests that 1-fluoro-2-aminonaphthalene may participate in various chemical reactions, including electrophilic aromatic substitution and nucleophilic reactions. Additionally, the compound may exhibit interesting physical properties, such as solubility in organic solvents and potential fluorescence, making it of interest in fields like materials science and organic synthesis. Its specific applications may vary, but compounds of this nature are often explored for their roles in pharmaceuticals, agrochemicals, and as intermediates in organic synthesis. Safety data should be consulted for handling and storage, as with any chemical substance.

CAS 14554-00-8

1-fluoro-2-aminonaphthalene

2-Naphthalenamine, 1-fluoro-

Ref: IN-DA001D5R

1-Fluoronaphthalen-2-amine

Ref: 54-PC100862

1-Fluoronaphthalen-2-amine

Ref: 10-F753236