• 1. Dissolution of cork biopolymers in biocompatible ionic liquids
  Helga Garcia,Rui Ferreira,Marija Petkovic,Jamie L. Ferguson,Maria C. Leit?o,H. Q. Nimal Gunaratne,Luís Paulo N. Rebelo Green Chem., 2010,12, 367-369
• 2. Excimer–monomer switch: a reaction-based approach for selective detection of fluoride?
  Qiao Song,Angela Bamesberger,Lingyun Yang,Haley Houtwed,Haishi Cao Analyst, 2014,139, 3588-3592
• 3. Excimer emission and magnetoluminescence of radical-based zinc(ii) complexes doped in host crystals?
  Shojiro Kimura,Tetsuro Kusamoto Chem. Commun., 2020,56, 11195-11198
• 4. Empowering microfluidics by micro-3D printing and solution-based mineral coating?
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• 5. EWOD-driven droplet microfluidic device integrated with optoelectronic tweezers as an automated platform for cellular isolation and analysis?
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• Solvents and Organic Chemicals Organic Compounds Benzenoids Phenols 1-hydroxy-2-unsubstituted benzenoids

4-(7-Methyloctyl)phenol: A Comprehensive Overview

4-(7-Methyloctyl)phenol is a unique chemical compound that has garnered significant attention in recent years due to its potential applications in various fields, including pharmaceuticals and material science. This compound, also known by its CAS Registry Number CAS NO 26543-97-5, belongs to the class of organic compounds and exhibits distinctive properties that make it a subject of interest for both academic and industrial researchers.

The structure of 4-(7-Methyloctyl)phenol consists of a phenolic ring substituted with a long alkyl chain. The presence of the hydroxyl group (-OH) on the aromatic ring imparts this compound with unique reactivity and solubility characteristics. This makes it a valuable precursor for various chemical reactions, particularly in the synthesis of more complex molecules.

One of the most notable aspects of CAS NO 26543-97-5 is its stability under varying conditions. Studies have shown that this compound retains its structural integrity even when exposed to elevated temperatures and harsh chemical environments, making it a robust candidate for use in demanding industrial processes.

In recent years, advancements in synthetic chemistry have enabled the large-scale production of 4-(7-Methyloctyl)phenol. These breakthroughs have not only enhanced the accessibility of this compound but also opened up new avenues for its application in diverse sectors. For instance, it has been explored as a building block in the development of advanced materials and pharmaceutical agents.

Research into the properties of CAS NO 26543-97-5 has revealed its potential as an effective chelating agent. This ability makes it a promising candidate for use in environmental remediation, particularly in the removal of heavy metal ions from contaminated water sources. Such applications highlight the compound's versatility and ecological significance.

Furthermore, 4-(7-Methyloctyl)phenol has been investigated for its role in drug delivery systems. Its hydrophilic nature combined with a long alkyl chain provides an ideal platform for the encapsulation of various therapeutic agents. This characteristic positions it as a potential vehicle for targeted drug delivery, enhancing the efficacy and minimizing side effects.

The compound's applications extend into the realm of polymers and composites. Owing to its unique structure, CAS NO 26543-97-5 has been utilized as a functional additive in polymer synthesis, imparting enhanced mechanical and thermal properties to the resulting materials. This makes it a valuable component in the development of high-performance polymers for industrial applications.

Recent studies have also explored the potential of 4-(7-Methyloctyl)phenol in catalysis. Its ability to act as both a substrate and a catalyst precursor has made it a subject of interest in green chemistry, where there is a growing emphasis on sustainable and environmentally friendly chemical processes.

In conclusion, CAS NO 26543-97-5 or 4-(7-Methyloctyl)phenol stands out as a versatile and valuable compound with a wide range of potential applications. Its unique properties, combined with the latest advancements in chemical synthesis and material science, position it at the forefront of innovation in various industries.

• 1638-22-8(4-Butylphenol)
• 1131-60-8(4-Cyclohexylphenol)
• 2589-78-8(Phenol, 4-hexadecyl-)
• 104-43-8(4-Dodecylphenol)
• 29799-07-3(4-(1-Adamantyl)phenol)
• 500-38-9(Nordihydroguaiaretic acid)
• 81936-33-6(4-(trans-4-Propylcyclohexyl)phenol)
• 14938-35-3(4-Pentylphenol)
• 99-71-8(4-(butan-2-yl)phenol)
• 140-66-9(4-Tert-Octylphenol)