56619-99-9 Usage
Chemical Structure
Spirocycle
Primary Use
Synthesis of pharmaceuticals and agrochemicals
Explanation
1,4-Dioxaspiro[4.4]nonane, 6-ethyl- is mainly used as a starting material or intermediate in the production of various pharmaceuticals and agrochemicals, which are chemicals used in the medical and agricultural industries.
Explanation
1,4-Dioxaspiro[4.4]nonane, 6-ethylserves as a building block in organic chemistry, meaning it can be used to create more complex molecules through chemical reactions.
Explanation
The compound has the potential to be used in the development of new materials and the research and development of novel compounds, which could have various applications in different industries.
Explanation
While the compound may have some industrial applications, its main use is in the production of various chemicals for scientific and commercial purposes, rather than being a direct component in industrial processes.
Building Block
Organic chemistry reactions
Potential Applications
Development of new materials and novel compounds
Industrial Uses
Limited, primarily focused on chemical production
Check Digit Verification of cas no
The CAS Registry Mumber 56619-99-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,6,1 and 9 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 56619-99:
(7*5)+(6*6)+(5*6)+(4*1)+(3*9)+(2*9)+(1*9)=159
159 % 10 = 9
So 56619-99-9 is a valid CAS Registry Number.
56619-99-9Relevant academic research and scientific papers
99.Transferts d'hydrogenes dans les cations radicaux ethylene-acetals derives de cyclopentanones et cyclohexanones
Audier, H. E.,Tabet, J. C.,Fetizon, M.
, p. 903 - 911 (2007/10/02)
Hydrogen Transfer during Decompositions of Molecular Ions of Acetals Derived from Substituted Cyclopentanones and Cyclohexanones.The isomerisation process of ethylene-acetal radical ions of low internal energy has been reinvestigated in more detail .The ring contraction of cyclohexane derivatives into methylcyclopentanes is quite general for these ions.The relative rates of H transfers to the C free resulting from C-C cleavage α to the acetal group plays the most important part in the mechanism.
