• 1. An aptamer-based keypad lock system?
  Yaqing Liu,Jiangtao Ren,Jing Li,Jiyang Liu,Erkang Wang Chem. Commun., 2012,48, 802-804
• 2. An ATP-selective, lanthanide complex luminescent probe?
  Xiao Liu,Jun Xu,Yinyun Lv,Wenyu Wu,Weisheng Liu,Yu Tang Dalton Trans., 2013,42, 9840-9846
• 3. An approach to biodegradable star polymeric architectures using disulfide coupling?
  Jingquan Liu,Huiyun Liu,Zhongfan Jia,Volga Bulmus,Thomas P. Davis Chem. Commun., 2008, 6582-6584
• 4. An antioxidative galactomannan extracted from Chinese Sesbania cannabina enhances immune activation of macrophage cells?
  Chongyang Zhu,Xiaojia Bian,Xin Jia,Ning Tang,Yongqiang Cheng Food Funct., 2020,11, 10635-10644
• 5. Aggregation dynamics, structure, and mechanical properties of bigels
  L. Di Michele,D. Fiocco,F. Varrato,E. Eiser,G. Foffi Soft Matter, 2014,10, 3633-3648

Comprehensive Guide to 4-Bromo-3,5-dichlorobenzaldehyde (CAS No. 120077-80-7): Properties, Applications, and Industry Insights

4-Bromo-3,5-dichlorobenzaldehyde (CAS No. 120077-80-7) is a halogenated aromatic aldehyde with significant relevance in organic synthesis and specialty chemical industries. This compound, characterized by its bromo and dichloro substituents on the benzene ring, serves as a versatile intermediate for pharmaceuticals, agrochemicals, and advanced materials. Its molecular structure, C₇H₃BrCl₂O, combines reactivity with stability, making it a sought-after building block in modern chemistry.

In recent years, the demand for halogenated benzaldehydes like 4-Bromo-3,5-dichlorobenzaldehyde has surged due to their role in synthesizing high-value compounds. Researchers frequently search for "synthesis methods for brominated aldehydes" or "applications of dichlorobenzaldehyde derivatives," reflecting growing interest in sustainable production techniques. The compound’s unique electronic properties, influenced by the electron-withdrawing effects of halogens, enable precise control in cross-coupling reactions—a topic trending in catalysis forums.

From an industrial perspective, CAS 120077-80-7 is pivotal in developing photoactive materials and liquid crystals, aligning with the global push for renewable energy technologies. A 2023 study highlighted its use in organic photovoltaics, addressing searches like "benzaldehyde derivatives in solar cells." Additionally, its role in pharmaceutical intermediates—particularly for antimicrobial agents—resonates with post-pandemic R&D priorities, as seen in queries such as "halogenated aromatics in drug design."

Environmental and regulatory considerations are also hot topics. While 4-Bromo-3,5-dichlorobenzaldehyde is not classified as hazardous under major frameworks, manufacturers emphasize "green halogenation techniques" to reduce waste. This aligns with the EU’s REACH guidelines and answers frequent searches on "eco-friendly bromination processes." Analytical methods like HPLC and GC-MS ensure purity (>98%), a critical parameter for buyers comparing "high-purity benzaldehyde suppliers."

Storage and handling recommendations for CAS 120077-80-7 include protection from light and moisture, with stability data showing no decomposition under standard conditions. Such details address practical queries like "how to store halogenated aldehydes." The compound’s melting point (92–94°C) and solubility in organic solvents are frequently cited in technical datasheets, catering to formulation scientists.

Innovation trends further spotlight 4-Bromo-3,5-dichlorobenzaldehyde in metal-organic frameworks (MOFs) and catalysis. A 2024 patent disclosed its use in asymmetric synthesis, tapping into the "chiral aldehyde applications" niche. As industries seek alternatives to traditional reagents, this compound’s balance of cost and functionality positions it as a sustainable choice—addressing SEO terms like "cost-effective aromatic aldehydes."

In conclusion, 4-Bromo-3,5-dichlorobenzaldehyde (CAS No. 120077-80-7) exemplifies the intersection of innovation and practicality in fine chemicals. Its multidisciplinary applications—from energy storage to precision medicine—make it a recurring subject in academic and industrial discourse, while evolving synthetic methods ensure its relevance in a greener chemical landscape.

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