2-Naphthalenecarbonitrile, 1-amino- is an organic compound characterized by the presence of a naphthalene ring system with a cyano group (–C≡N) and an amino group (–NH2) attached to the carbon framework. This compound typically exhibits a solid state at room temperature and is known for its aromatic properties due to the conjugated pi-electron system of the naphthalene structure. The amino group can participate in hydrogen bonding, influencing its solubility and reactivity. As a nitrile, it may also exhibit reactivity typical of such functional groups, including nucleophilic addition reactions. The compound is of interest in various fields, including organic synthesis and materials science, due to its potential applications in pharmaceuticals and as an intermediate in chemical reactions. Safety data sheets should be consulted for handling and storage guidelines, as compounds with amino and nitrile functionalities may pose health risks if not managed properly.

2-Naphthalenecarbonitrile, 1-amino-

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1-Amino-2-naphthonitrile

1-Amino-2-naphthonitrile is a chemical compound that is used in the production of 4,4'-diaminodiphenyl ether. It is also a precursor to the synthesis of 1-aminoanthracene, which is an electrophile and has been shown to induce cancer in experimental animals. The skeleton of 1-amino-2-naphthonitrile contains a phenyl group and can be detected using x-ray crystallography. This compound also forms carbocations during reactions with carbon disulfide. Carbon disulfide reacts with 1-amino-2-naphthonitrile and yields methyl ketones. The methyl ketones are then reacted with ethylene glycol to yield 4,4'-diaminodiphenyl ether.

CAS 3100-67-2: 2-Naphthalenecarbonitrile, 1-amino-

2-Naphthalenecarbonitrile, 1-amino-

Ref: IN-DA0031WU

1-Amino-2-naphthonitrile

Ref: 54-OR91965

1-Amino-2-naphthonitrile

Ref: 10-F499074

1-Amino-2-naphthonitrile

Ref: 3D-DAA10067