1,2-Bis(p-bromophenoxy)octane is an organic compound characterized by its structure, which features a central octane chain with two p-bromophenoxy groups attached at the first and second carbon positions. This compound is notable for its brominated aromatic rings, which can enhance its reactivity and potential applications in various fields, including materials science and pharmaceuticals. The presence of bromine atoms contributes to its hydrophobic nature and may impart flame-retardant properties. Additionally, the compound's molecular structure suggests potential for interactions with biological systems, making it of interest in medicinal chemistry. Its synthesis typically involves the reaction of octane derivatives with p-bromophenol under specific conditions to ensure the formation of the ether linkages. As with many brominated compounds, considerations regarding environmental impact and toxicity are essential, particularly in terms of persistence and bioaccumulation. Overall, 1,2-bis(p-bromophenoxy)octane exemplifies a class of compounds that bridge organic chemistry and practical applications, warranting further investigation into its properties and uses.

1,2-BIS-(P-BROMOPHENOXY)OCTANE

117499-25-9: 1,2-Bis(p-bromophenoxy)octane is an organic compound characterized by its structure, which features a central octane chain with two p-bromophenoxy groups attached at the first and second carbon positions. This compound is notable for its brominated aromatic rings, which can enhance its reactivity and potential applications in various fields, including materials science and pharmaceuticals. The presence of bromine atoms contributes to its hydrophobic nature and may impart flame-retardant properties. Additionally, the compound's molecular structure suggests potential for interactions with biological systems, making it of interest in medicinal chemistry. Its synthesis typically involves the reaction of octane derivatives with p-bromophenol under specific conditions to ensure the formation of the ether linkages. As with many brominated compounds, considerations regarding environmental impact and toxicity are essential, particularly in terms of persistence and bioaccumulation. Overall, 1,2-bis(p-bromophenoxy)octane exemplifies a class of compounds that bridge organic chemistry and practical applications, warranting further investigation into its properties and uses.

CAS 117499-25-9

1,2-BIS-(P-BROMOPHENOXY)OCTANE

1,8-Bis(4-bromophenoxy)octane

Ref: TR-B802896