5-Bromonaphthalene-1-carboxylic acid is an aromatic compound characterized by the presence of a bromine atom and a carboxylic acid functional group attached to a naphthalene ring system. This compound features a naphthalene backbone, which consists of two fused benzene rings, providing it with significant stability and hydrophobic characteristics. The bromine substituent introduces both electronegativity and steric effects, influencing the compound's reactivity and solubility. The carboxylic acid group (-COOH) imparts acidic properties, allowing for potential hydrogen bonding and increased solubility in polar solvents. This compound is typically used in organic synthesis, serving as an intermediate in the production of various pharmaceuticals, agrochemicals, and dyes. Its reactivity can be attributed to the electrophilic nature of the aromatic system, making it suitable for further functionalization. Additionally, the presence of the bromine atom can facilitate cross-coupling reactions, enhancing its utility in synthetic organic chemistry. Overall, 5-bromonaphthalene-1-carboxylic acid is a versatile compound with applications in various chemical fields.

5-bromonaphthalene-1-carboxylic acid

5-Bromo-1-naphthoic acid

5-Bromo-1-naphthoic acid (5-BNAA) is a photoactive agent that belongs to the group of anti-tumor agents. It has been shown to have a strong enhancing effect on the production of ethyl esters, which are intermediates in the biosynthesis of naphthalene. 5-BNAA can be used as an anti-cancer drug, but it also has a cytotoxic effect on blood vessels and erythrocytes. 5-BNAA blocks nucleophilic reactions by binding to DNA and RNA, thereby inhibiting protein synthesis. This drug also acts as a surfactant by increasing the surface tension of water and preventing coagulation.

CAS 16726-67-3: 5-bromonaphthalene-1-carboxylic acid

5-Bromo-1-naphthoic acid

Ref: IN-DA007W60

5-Bromo-1-naphthoic acid

Ref: 10-F214702

5-Bromo-1-naphthoic acid

Ref: 3D-FB33073

5-Bromo-1-naphthoic acid

Ref: 54-OR74982