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  Priyambada Nayak,Tanmaya Badapanda,Anil Kumar Singh,Simanchalo Panigrahi RSC Adv., 2017,7, 16319-16331
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  S. Amaresh,K. Karthikeyan,K. J. Kim,Y. S. Lee RSC Adv., 2014,4, 23107-23115
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  Luke L. Lairson,Warren W. Wakarchuk Chem. Commun., 2007, 365-367
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• Solvents and Organic Chemicals Organic Compounds Lipids and lipid-like molecules Fatty Acyls Fatty acids and conjugates Halogenated fatty acids

Compound CAS No. 952584-86-0: 4-(2,2,3,3,4,4,4-Heptafluorobutoxy)-4-oxobut-2-enoic Acid

The compound with CAS No. 952584-86-0, known as 4-(2,2,3,3,4,4,4-heptafluorobutoxy)-4-oxobut-2-enoic acid, is a highly fluorinated organic compound with unique chemical properties. This compound belongs to the class of enoic acids and features a heptafluorobutoxy group attached to the central carbon chain. The presence of multiple fluorine atoms in its structure contributes to its distinct physical and chemical characteristics.

Fluorinated compounds have gained significant attention in recent years due to their applications in various fields such as pharmaceuticals, agrochemicals, and materials science. The heptafluorobutoxy group in this compound is particularly notable for its high stability and lipophilicity. These properties make it a valuable building block for the synthesis of advanced materials and bioactive molecules.

Recent studies have highlighted the potential of heptafluorobutoxy-containing compounds in drug design. The fluorine atoms in the structure enhance the molecule's ability to interact with biological targets through various mechanisms such as hydrogen bonding and π–π interactions. This has led to increased interest in using this compound as a precursor for developing novel therapeutic agents.

The synthesis of CAS No. 952584-86-0 involves a multi-step process that typically includes fluorination reactions and subsequent functional group transformations. Researchers have explored various methods to optimize the synthesis pathway, ensuring high yields and purity of the final product. These advancements have been documented in recent publications focusing on fluorinated organic chemistry.

In terms of applications, 4-(2,2,3,3,4,4,4-heptafluorobutoxy)-4-oxobut-2-enoic acid has shown promise in the development of advanced polymers and coatings. Its high thermal stability and resistance to environmental degradation make it an ideal candidate for use in high-performance materials. Additionally, its role as an intermediate in the synthesis of bioactive compounds has been extensively studied.

Recent research has also focused on understanding the environmental impact of this compound. Studies have shown that while it exhibits excellent chemical stability under normal conditions, it can undergo degradation under specific environmental conditions such as UV light exposure or microbial activity. This knowledge is crucial for assessing its safety and sustainability in industrial applications.

The unique combination of properties exhibited by CAS No. 952584-86-0 makes it a valuable compound for both academic research and industrial applications. Its ability to serve as a versatile building block for synthesizing complex molecules has positioned it at the forefront of modern organic chemistry.

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