2-Bromonaphthalen-1-amine, with the CAS number 771-14-2, is an organic compound that features a naphthalene ring substituted with both a bromine atom and an amino group. This compound is characterized by its aromatic structure, which contributes to its stability and reactivity. The presence of the bromine atom introduces electrophilic characteristics, making it a potential candidate for further chemical reactions, such as nucleophilic substitutions or coupling reactions. The amino group (-NH2) enhances its solubility in polar solvents and can participate in hydrogen bonding, influencing its physical properties. Typically, 2-bromonaphthalen-1-amine appears as a solid at room temperature and may exhibit moderate toxicity, necessitating careful handling. Its applications can range from use in organic synthesis to serving as an intermediate in the production of dyes, pharmaceuticals, and agrochemicals. As with many aromatic amines, it is important to consider its environmental impact and potential health hazards during use and disposal.

2-bromonaphthalen-1-amine

771-14-2: 1-Naphthalenamine, 2-Bromo-,  2-Bromonaphthalen-1-amine

1-Amino-2-bromonaphthalene

2-Bromonaphthalen-1-amine

1-Amino-2-bromonaphthalene is a synthetic compound that is used as a recyclable reagent. It has been shown to have an inhibitory effect on cancer cells and tissue, stabilizing the DNA molecule and preventing it from being broken down. 1-Amino-2-bromonaphthalene also has affinity for cancer cells and stabilizes the cell membrane by inhibiting phosphonate degradation. The drug has been envisaged as a potential candidate for cancer therapy due to its ability to stabilize the cell membrane and inhibit phosphonates, which are involved in cell division.

CAS 771-14-2: 2-bromonaphthalen-1-amine

1-Amino-2-bromonaphthalene

Ref: 3B-B3411

2-Bromonaphthalen-1-amine

Ref: 10-F318213

2-Bromonaphthalen-1-amine

Ref: 54-OR938748

2-Bromonaphthalen-1-amine

Ref: IN-DA003DXH

1-Amino-2-bromonaphthalene

Ref: 3D-AAA77114