1-Naphthalenecarbonitrile, 5-amino- is an organic compound characterized by the presence of a naphthalene ring system substituted with a carbonitrile group and an amino group. The compound features a nitrile functional group (-C≡N) attached to the carbon of the naphthalene, which contributes to its reactivity and potential applications in organic synthesis. The amino group (-NH2) is located at the 5-position of the naphthalene ring, influencing the compound's properties, such as solubility and reactivity. This compound is typically a solid at room temperature and may exhibit moderate polarity due to the presence of both the amino and nitrile groups. It can participate in various chemical reactions, including nucleophilic substitutions and coupling reactions, making it valuable in the synthesis of pharmaceuticals and agrochemicals. Additionally, its structural features may allow for interactions with biological systems, suggesting potential applications in medicinal chemistry. Safety and handling precautions should be observed, as with many organic compounds, due to potential toxicity or reactivity.

1-Naphthalenecarbonitrile, 5-amino-

5-Amino-1-naphthonitrile is a solid that belongs to the class of heterocycles. It is a monosubstituted naphthalene with an amine group. 5-Amino-1-naphthonitrile can be used as a probe for reactive groups in organic compounds and can also be used to quantify acidity constants. This compound has been shown to have linear regression and is scalable, which makes it useful in research studies. The synthesis of 5-amino-1-naphthonitrile requires the use of dimethylformamide and acetonitrile, which are both scalable chemicals.
5-Amino-1-naphthonitrile can be used to form pyridine derivatives, which are important for pharmaceuticals, pesticides, and herbicides.

CAS 72016-73-0: 1-Naphthalenecarbonitrile, 5-amino-

5-Amino-1-naphthonitrile

Ref: 3D-XCA01673

5-Amino-1-naphthonitrile

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5-Amino-1-naphthonitrile

Ref: 54-OR302254

5-Amino-1-naphthonitrile

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