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3-Bromo-5-Iodo-4-Methoxybenzaldehyde (CAS No. 1356113-31-9)

3-Bromo-5-Iodo-4-Methoxybenzaldehyde is a highly specialized aromatic aldehyde compound with the CAS registry number 1356113-31-9. This compound is characterized by its unique substitution pattern, featuring a bromine atom at the 3-position, an iodine atom at the 5-position, and a methoxy group at the 4-position of the benzene ring. The presence of these substituents imparts distinctive chemical and physical properties to the molecule, making it a valuable compound in various research and industrial applications.

The synthesis of 3-Bromo-5-Iodo-4-Methoxybenzaldehyde involves a series of carefully designed organic reactions. Typically, the starting material is a substituted benzaldehyde derivative, which undergoes nucleophilic substitution or electrophilic aromatic substitution to introduce the bromine and iodine atoms. The methoxy group is often introduced via O-methylation or through protection-deprotection strategies. The exact synthetic pathway may vary depending on the specific substituents and their reactivity, but modern methodologies ensure high yields and purity of the final product.

Recent studies have highlighted the importance of 3-Bromo-5-Iodo-4-Methoxybenzaldehyde in drug discovery and development. The compound's unique electronic properties make it an attractive candidate for targeting specific biological pathways. For instance, researchers have explored its potential as a lead compound in anti-cancer drug development due to its ability to modulate key enzymes involved in cell proliferation and apoptosis. Additionally, its iodine and bromine substituents provide opportunities for further functionalization, enabling the creation of derivatives with enhanced bioactivity.

In terms of physical properties, 3-Bromo-5-Iodo-4-Methoxybenzaldehyde exhibits a melting point of approximately 220°C under standard conditions. Its solubility in common organic solvents such as dichloromethane and ethyl acetate makes it suitable for various analytical techniques, including high-performance liquid chromatography (HPLC) and nuclear magnetic resonance (NMR) spectroscopy. The compound's UV-vis spectrum reveals strong absorption bands in the ultraviolet region, which can be exploited for sensing applications.

From an environmental perspective, 3-Bromo-5-Iodo-4-Methoxybenzaldehyde has been studied for its biodegradability and ecotoxicological effects. Research indicates that under aerobic conditions, the compound undergoes microbial degradation through oxidative pathways, resulting in the formation of less toxic byproducts. However, further studies are required to fully understand its long-term impact on aquatic ecosystems.

Looking ahead, 3-Bromo-5-Iodo-4-Methoxybenzaldehyde holds promise in advanced materials science applications. Its ability to form stable coordination complexes with transition metals makes it a potential candidate for use in catalysis and sensor technologies. For example, recent advancements have demonstrated its utility as a sensing platform for detecting trace amounts of heavy metals in water samples.

In conclusion, 3-Bromo-5-Iodo-4-Methoxybenzaldehyde (CAS No. 1356113-31) is a versatile compound with diverse applications across multiple scientific disciplines. Its unique chemical structure, combined with cutting-edge research findings, positions it as a valuable tool in modern chemistry and materials science.

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• 145489-48-1(Ethanone, 1-(5-bromo-2-hydroxy-3-iodo-4-phenoxyphenyl)-)
• 708272-90-6(5-bromo-2-ethoxy-3-iodobenzaldehyde)