Naphthalene, 1-bromo-2-ethoxy- (CAS 50389-70-3) is an organic compound characterized by its structure, which includes a naphthalene ring substituted with a bromine atom and an ethoxy group. This compound typically exhibits the properties associated with aromatic compounds, such as stability and a tendency to undergo electrophilic substitution reactions. The presence of the bromine atom introduces a halogen functionality, which can enhance reactivity, particularly in nucleophilic substitution reactions. The ethoxy group contributes to the compound's solubility in organic solvents and can influence its physical properties, such as boiling and melting points. Naphthalene derivatives are often used in various applications, including as intermediates in the synthesis of dyes, pharmaceuticals, and agrochemicals. Additionally, the compound may exhibit biological activity, making it of interest in medicinal chemistry. Safety considerations should be taken into account, as many naphthalene derivatives can be toxic or harmful to the environment. Overall, Naphthalene, 1-bromo-2-ethoxy- is a versatile compound with significant implications in both industrial and research settings.

Naphthalene, 1-bromo-2-ethoxy-

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1-Bromo-2-ethoxynaphthalene

1-Bromo-2-ethoxynaphthalene is a synthetic organic compound that has been shown to have environmentally favorable properties. It is a pyridine derivative with a hydroxy group at the 1-position. The micellar solubility of 1-bromo-2-ethoxynaphthalene is higher than that of other pyridines, which may be due to its electron donating effect on the electron rich ring.

CAS 50389-70-3: Naphthalene, 1-bromo-2-ethoxy-

1-Bromo-2-ethoxynaphthalene

Ref: IN-DA00DGDM

1-Bromo-2-ethoxynaphthalene

Ref: 10-F401128

1-Bromo-2-ethoxynaphthalene

Ref: 3D-ACA38970