Benzo[b]naphtho[2,3-d]furan, with the CAS number 243-42-5, is a polycyclic aromatic compound characterized by its fused ring structure, which consists of multiple aromatic rings. This compound features a furan ring fused to a naphthalene system, contributing to its complex aromatic character. It is typically a solid at room temperature and may exhibit a range of physical properties, including a specific melting point and solubility characteristics that depend on the solvent used. Benzo[b]naphtho[2,3-d]furan is of interest in various fields, including organic chemistry and materials science, due to its potential applications in organic electronics and as a building block for more complex molecular architectures. Its chemical behavior is influenced by the presence of the furan moiety, which can participate in various chemical reactions, including electrophilic aromatic substitution. Additionally, like many polycyclic aromatic hydrocarbons, it may exhibit fluorescence and has implications in environmental chemistry due to its potential formation in combustion processes. Safety and handling precautions are essential, as with many organic compounds, to mitigate any health risks associated with exposure.

Benzo[b]naphtho[2,3-d]furan

243-42-5: Benzo[b]naphtho[2,3-d]furan, with the CAS number 243-42-5, is a polycyclic aromatic compound characterized by its fused ring structure, which consists of multiple aromatic rings. This compound features a furan ring fused to a naphthalene system, contributing to its complex aromatic character. It is typically a solid at room temperature and may exhibit a range of physical properties, including a specific melting point and solubility characteristics that depend on the solvent used. Benzo[b]naphtho[2,3-d]furan is of interest in various fields, including organic chemistry and materials science, due to its potential applications in organic electronics and as a building block for more complex molecular architectures. Its chemical behavior is influenced by the presence of the furan moiety, which can participate in various chemical reactions, including electrophilic aromatic substitution. Additionally, like many polycyclic aromatic hydrocarbons, it may exhibit fluorescence and has implications in environmental chemistry due to its potential formation in combustion processes. Safety and handling precautions are essential, as with many organic compounds, to mitigate any health risks associated with exposure.

CAS 243-42-5

Benzo[b]naphtho[2,3-d]furan

Naphtho[2,3-b]benzofuran

Ref: TR-B131165