CAS 57133-55-8

1,4-Dioxaspiro[4.5]decane-6-acetic acid, ethyl ester

Description:

1,4-Dioxaspiro[4.5]decane-6-acetic acid, ethyl ester, with the CAS number 57133-55-8, is a chemical compound characterized by its unique spirocyclic structure, which incorporates a dioxane moiety. This compound features a spiro linkage that connects two cyclic systems, contributing to its rigidity and potential for specific interactions in biological systems. The presence of an ethyl ester functional group suggests that it may exhibit moderate lipophilicity, influencing its solubility and permeability in various environments. Additionally, the acetic acid component indicates potential reactivity, particularly in esterification or hydrolysis reactions. The compound's structural features may confer interesting properties, such as potential applications in medicinal chemistry or materials science, where spiro compounds are often explored for their unique conformational and electronic characteristics. Overall, 1,4-Dioxaspiro[4.5]decane-6-acetic acid, ethyl ester represents a fascinating subject for further research, particularly in the context of its synthesis, reactivity, and potential applications.

Formula: C₁₂H₂₀O₄

Ethyl 2-{1,4-dioxaspiro[4.5]decan-6-yl}acetate

CAS: 57133-55-8

Ethyl 2-{1,4-dioxaspiro[4.5]decan-6-yl}acetate is an organic compound that can be synthesized by the allylation of the corresponding acid chloride and cyclic ester with ethyl bromoacetate. It is a surrogate for halides in biological studies and has been used as a building block for statins. This compound was also used to synthesize azaphilones through an asymmetric synthesis approach. Ethyl 2-{1,4-dioxaspiro[4.5]decan-6-yl}acetate is able to form amines by reacting with ammonia or ammonium hydroxide, which makes it useful in the synthesis of drugs such as antihistamines and antihypertensives. Ethyl 2-{1,4-dioxaspiro[4.5]decan-6-yl}acetate can also be used as a precursor

Formula: C₁₂H₂₀O₄

Purity: Min. 95%

Molecular weight: 228.28 g/mol

Ref: 3D-HCA13355