• 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. Exciplex emission from the mixed dimer of naphthalene and 2-cyanonaphthalene in a supersonic jet
  Aloke Das,K. K. Mahato,Chayan K. Nandi,Tapas Chakraborty,Shridhar R. Gadre,Nikhil A. Gokhale Phys. Chem. Chem. Phys., 2002,4, 2162-2168
• 3. Fe3O4@PANI: a magnetic polyaniline nanomaterial for highly efficient and handy enrichment of intact N-glycopeptides??
  Zhizhen Lai,Mo Zhang,Jinyu Zhou,Tianjing Chen,Dan Li,Xuejing Shen,Jia Liu,Jiang Zhou,Zhili Li Analyst, 2021,146, 4261-4267
• 4. Excellent mechanical performance and enhanced dielectric properties of OBC/SiO2 elastomeric nanocomposites: effect of dispersion of the SiO2 nanoparticles?
  Xing Zhao,Lu Bai,Rui-Ying Bao,Zheng-Ying Liu,Ming-Bo Yang,Wei Yang RSC Adv., 2017,7, 46297-46305
• 5. Estimation of activation energy for electroporation and pore growth rate in liquid crystalline and gel phases of lipid bilayers using molecular dynamics simulations?
  Amit Kumar Majhi,Subbarao Kanchi,V. Venkataraman,K. G. Ayappa,Prabal K. Maiti Soft Matter, 2015,11, 8632-8640

• Solvents and Organic Chemicals Organic Compounds Organic oxygen compounds Organooxygen compounds Acetals
• Solvents and Organic Chemicals Organic Compounds Organic oxygen compounds Organooxygen compounds Ethers Acetals

Ethyl 2-{1,4-Dioxaspiro[4.5]Decan-8-yl}Acetate: A Comprehensive Overview

Ethyl 2-{1,4-dioxaspiro[4.5]decan-8-yl}acetate, also known by its CAS number 62141-26-8, is a unique organic compound with a complex structure that has garnered attention in various scientific and industrial applications. This compound belongs to the class of spiro compounds, which are characterized by two rings sharing a single atom. The spiro structure in this molecule is further modified by the presence of a dioxane ring and an acetate group, making it a versatile compound with potential applications in pharmaceuticals, materials science, and advanced chemical synthesis.

The molecular structure of ethyl 2-{1,4-dioxaspiro[4.5]decan-8-yl}acetate is defined by its spirocyclic framework. The spiro ring system consists of a five-membered ring (spiro[4.5]) fused with a six-membered dioxane ring. This arrangement creates a rigid yet flexible structure that can accommodate various functional groups. The acetate group attached to the spiro system introduces additional reactivity and solubility properties, making it suitable for a wide range of chemical reactions.

Recent studies have highlighted the potential of spiro compounds like ethyl 2-{1,4-dioxaspiro[4.5]decan-8-yl}acetate in drug delivery systems. Researchers have explored the use of this compound as a precursor for bioactive molecules due to its ability to form stable ester linkages and its compatibility with various functionalization techniques. Additionally, the compound's unique electronic properties have been leveraged in the development of advanced materials, such as stimuli-responsive polymers and self-healing materials.

In terms of synthesis, ethyl 2-{1,4-dioxaspiro[4.5]decan-8-yl}acetate can be prepared through a variety of methods, including ring-closing metathesis and traditional organic synthesis techniques. The choice of synthesis method depends on the desired scale of production and the specific requirements of the application. Recent advancements in catalytic methods have made it possible to achieve higher yields and better control over the stereochemistry of the product.

The physical properties of ethyl 2-{1,4-dioxaspiro[4.5]decan-8-yl}acetate include a melting point of approximately 70°C and a boiling point around 300°C under standard conditions. Its solubility in common organic solvents such as dichloromethane and ethyl acetate makes it easy to handle in laboratory settings. The compound is also relatively stable under ambient conditions, though it may undergo hydrolysis under acidic or basic conditions.

One of the most promising applications of ethyl 2-{1,4-dioxaspiro[4.5]decan-8-yl}acetate is in the field of polymer chemistry. Scientists have investigated its use as a building block for synthesizing novel polymers with tailored properties. For instance, its ability to form cross-linked networks has been exploited in the development of high-performance adhesives and coatings that exhibit excellent mechanical strength and thermal stability.

Moreover, ethyl 2-{1,4-dioxaspiro[4.5]decan-8-yl}acetate has shown potential in green chemistry initiatives due to its compatibility with environmentally friendly reaction conditions. Researchers have demonstrated that this compound can be synthesized using renewable feedstocks and catalyzed by enzymes or other biocompatible catalysts, reducing the environmental footprint associated with traditional chemical manufacturing processes.

In conclusion, ethyl 2-{1,4-dioxaspiro[4.5]decan-8-yl}acetate (CAS No: 62141-26-8) is a versatile compound with a rich structural diversity that opens up numerous possibilities for innovation across various industries. Its unique properties make it an invaluable tool for scientists and engineers seeking to develop advanced materials and sustainable chemical processes.

• 6624-91-5(1,3-Dioxolane-2-propanoicacid, 2-methyl-, cyclohexyl ester)
• 646038-29-1(1,4-Dioxaspiro[4.5]decane-7-acetic acid, methyl ester, (7S)-)
• 317338-46-8(methyl 2-{1,4-dioxaspiro[4.5]decan-8-yl}acetate)
• 1489-97-0(Ethyl 1,4-dioxaspiro[4.5]decane-8-carboxylate)
• 226916-27-4((1'R,3a'R,4a'R,8a'R,9'S,9a'R)-1'-Methyl-3'-oxodecahydro-1'H-spiro[[1,3]dioxolane-2,6'-naphtho[2,3-c]furan]-9'-carboxylic acid)
• 57133-55-8(Ethyl 2-{1,4-Dioxaspiro4.5decan-6-yl}acetate)
• 93306-08-2(ETHYL 1,4-DIOXASPIRO[4.4]NONANE-7-ACETATE)
• 88152-69-6(1,4,8,11-Tetraoxadispiro[4.1.4.3]tetradecane-13-carboxylic acid, ethyl ester)
• 141380-53-2(1,4-Dioxaspiro[4.5]decane-7-hexanoic acid, 9,9-dimethyl-, methyl ester)
• 73831-19-3(ethyl cis-7-methyl-1,4-dioxaspiro[4.5]decane-8-carboxylate)