• 1. Acentric and chiral heterometallic inorganic–organic hybrid frameworks mediated by alkali or alkaline earth ions: synthesis and NLO properties
  Huabin Zhang,Shaowu Du CrystEngComm, 2014,16, 4059-4068
• 2. An ionic liquid-mesoporous silica blend as a novel adsorbent for the adsorption and recovery of palladium ions, and its applications in continuous flow study and as an industrial catalyst?
  Shivani Sharma,Chia-Ming Wu,Ranjit T. Koodali,N. Rajesh RSC Adv., 2016,6, 26668-26678
• 3. An arsenic trioxide nanoparticle prodrug (ATONP) potentiates a therapeutic effect on an aggressive hepatocellular carcinoma model via enhancement of intratumoral arsenic accumulation and disturbance of the tumor microenvironment?
  Xin Fu,Qing-rong Liang,Rong-guang Luo,Yan-shu Li,Xiao-ping Xiao,Lu-lu Yu,Wen-zhe Shan,Guang-qin Fan J. Mater. Chem. B, 2019,7, 3088-3099
• 4. An aptamer-based keypad lock system?
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• 5. An approach to biodegradable star polymeric architectures using disulfide coupling?
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• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Benzofurans Benzofurans
• Solvents and Organic Chemicals Organic Compounds Organoheterocyclic compounds Benzofurans

Comprehensive Overview of 7-Methoxy-1-benzofuran-2-carbaldehyde (CAS No. 88234-77-9): Properties, Applications, and Research Insights

7-Methoxy-1-benzofuran-2-carbaldehyde (CAS No. 88234-77-9) is a specialized organic compound belonging to the benzofuran family, characterized by its unique methoxy and aldehyde functional groups. This compound has garnered significant attention in pharmaceutical and material science research due to its versatile chemical structure. With a molecular formula of C₁₀H₈O₃, it serves as a key intermediate in synthesizing bioactive molecules, including potential antioxidants and anti-inflammatory agents, aligning with current trends in drug discovery and green chemistry.

Recent studies highlight the role of 7-methoxy-1-benzofuran-2-carbaldehyde in flavor and fragrance applications, where its aromatic properties are exploited for creating complex olfactory profiles. Researchers are also exploring its utility in organic electronics, particularly in designing light-emitting diodes (LEDs) and photovoltaic materials, addressing the growing demand for sustainable energy solutions. The compound’s low toxicity and biodegradability further enhance its appeal in eco-conscious industries.

From a synthetic perspective, CAS No. 88234-77-9 is often derived via Vilsmeier-Haack formylation or oxidative coupling reactions, methodologies frequently searched in academic databases. Its crystallographic data and spectroscopic properties (e.g., NMR and IR spectra) are well-documented, making it a reference compound for analytical chemists. The rise of AI-driven molecular modeling has further propelled interest in predicting its reactivity and optimizing synthesis routes, a topic trending in computational chemistry forums.

In the context of consumer safety, regulatory bodies classify 7-methoxy-1-benzofuran-2-carbaldehyde as non-hazardous under standard handling conditions, though proper laboratory protocols are recommended. Its compatibility with green solvents like ethanol and water aligns with the global shift toward sustainable manufacturing, a frequently searched term in industrial chemistry circles. Additionally, its stability under ambient conditions makes it a practical choice for long-term storage.

Future research directions for 88234-77-9 may focus on its potential in nanotechnology and bioconjugation, areas gaining traction in multidisciplinary studies. As the scientific community prioritizes carbon-neutral processes, this compound’s derivatization pathways could contribute to circular economy initiatives. For those seeking high-purity samples, reputable suppliers often provide GC-MS and HPLC certifications, ensuring compliance with ISO standards.

• 43071-52-9(2-Acetyl-7-methoxybenzofuran)
• 58583-72-5(1-(7-ethoxy-1-benzofuran-2-yl)ethan-1-one)
• 64466-48-4(Ethanone,1-(6,7-dimethoxy-2-benzofuranyl)-)
• 64418-91-3(2-Benzofurancarboxaldehyde,5-hydroxy-)
• 23145-19-9(5-methoxy-1-benzofuran-2-carbaldehyde)
• 4790-79-8(7-Methoxybenzofuran-2-carboxylic acid)
• 229971-93-1(Curcapital)
• 206559-61-7(7-ethoxy-1-benzofuran-2-carboxylic acid)
• 29025-30-7(7-methoxy-2-methyl-Benzofuran)
• 53020-46-5(2-Benzofurancarboxamide, 7-methoxy-)