2-Acetyl-6-bromonaphthalene is an organic compound characterized by its naphthalene backbone substituted with an acetyl group and a bromine atom. It features a molecular structure that includes a bromine atom at the 6-position and an acetyl group at the 2-position of the naphthalene ring. This compound typically appears as a solid at room temperature and is known for its aromatic properties, which contribute to its stability and reactivity. The presence of the acetyl group introduces a carbonyl functionality, making it a potential candidate for various chemical reactions, including Friedel-Crafts acylation and nucleophilic substitutions. Additionally, the bromine substituent can serve as a site for further functionalization, enhancing its utility in synthetic organic chemistry. 2-Acetyl-6-bromonaphthalene is often used in research and industrial applications, particularly in the synthesis of more complex organic molecules and in studies related to its electronic and photophysical properties. Safety precautions should be observed when handling this compound, as it may pose health risks typical of halogenated organic substances.

2-Acetyl-6-bromonaphthalene

1590-25-6: 2-Acetyl-6-bromonaphthalene is an organic compound characterized by its naphthalene backbone substituted with an acetyl group and a bromine atom. It features a molecular structure that includes a bromine atom at the 6-position and an acetyl group at the 2-position of the naphthalene ring. This compound typically appears as a solid at room temperature and is known for its aromatic properties, which contribute to its stability and reactivity. The presence of the acetyl group introduces a carbonyl functionality, making it a potential candidate for various chemical reactions, including Friedel-Crafts acylation and nucleophilic substitutions. Additionally, the bromine substituent can serve as a site for further functionalization, enhancing its utility in synthetic organic chemistry. 2-Acetyl-6-bromonaphthalene is often used in research and industrial applications, particularly in the synthesis of more complex organic molecules and in studies related to its electronic and photophysical properties. Safety precautions should be observed when handling this compound, as it may pose health risks typical of halogenated organic substances.

CAS 1590-25-6

2-Acetyl-6-bromonaphthalene

Ethanone, 1-(6-bromo-2-naphthalenyl)-

Ref: IN-DA001R38

1-(6-Bromonaphthalen-2-yl)ethanone

Ref: 54-OR79596

1-(6-Bromonaphthalen-2-yl)ethanone

Ref: 10-F460323