6-Bromo-2,3-naphthalenedicarbonitrile is an organic compound characterized by its naphthalene backbone, which is substituted with a bromine atom and two cyano groups. The presence of the bromine atom introduces a halogen, which can influence the compound's reactivity and solubility. The cyano groups (-C≡N) are strong electron-withdrawing groups, contributing to the compound's overall polarity and potential applications in various chemical reactions, including nucleophilic substitutions and as intermediates in organic synthesis. This compound is typically used in research and development, particularly in the fields of materials science and pharmaceuticals, due to its unique electronic properties and ability to form coordination complexes. Additionally, the structure suggests potential for applications in dye chemistry and as a building block for more complex organic molecules. Safety data should be consulted, as compounds containing bromine and cyano groups can pose health risks and require careful handling.

6-Bromo-2,3-naphthalenedicarbonitrile

70484-02-5: 2,3-Naphthalenedicarbonitrile, 6-bromo-, 6-Bromo-2,3-dicyanonaphthalene, 6-Bromo-2,3-naphthalenedicarbonitrile, 6-Bromonaphthalene-2,3-Dicarbonitrile

6-BROMO-2,3-DICYANONAPHTHALENE

6-Bromonaphthalene-2,3-dicarbonitrile

6-Bromo-2,3-dicyanonaphthalene (6-BCN) is a carboxylate that has been shown to be photochemically reactive. It has been used in the detection of cervical cancer, where 6-BCN was used as a fluorescent probe and showed an excellent sensitivity with very low background.

CAS 70484-02-5: 6-Bromo-2,3-naphthalenedicarbonitrile

6-BROMO-2,3-DICYANONAPHTHALENE

Ref: IN-DA003N3M

6-Bromonaphthalene-2,3-dicarbonitrile

Ref: 10-F618901

6-Bromo-2,3-dicyanonaphthalene

Ref: 3D-FB62503

6-Bromo-2,3-Dicyanonaphthalene

Ref: 54-OR1026660

6-Bromo-2,3-dicyanonaphthalene

Ref: 3B-B1390