105018-99-3 Usage
Explanation
The molecular formula represents the number of atoms of each element present in a molecule. In this case, the compound has 10 carbon (C) atoms, 16 hydrogen (H) atoms, and 2 oxygen (O) atoms.
2. Bicyclic organic compound
Explanation
The compound has two rings in its structure, making it a bicyclic compound. It is also organic, meaning it primarily consists of carbon and hydrogen atoms.
3. Spiro ring system
Explanation
The two rings in the compound are connected by a shared carbon atom, forming a spiro ring system. This unique arrangement of rings contributes to the compound's properties and potential applications.
4. Used in pharmaceuticals
Explanation
Due to its unique structure, 1,4-Dioxaspiro[4.5]dec-6-ene, 7-methylcan be used as a building block in the synthesis of various pharmaceutical compounds.
5. Used in perfumes and personal care products
Explanation
The compound's fragrance properties make it suitable for use as an ingredient in perfumes and personal care products.
6. Potential applications in medicinal chemistry and drug development
Explanation
The structural features of the compound make it a promising candidate for further research and development in the field of medicinal chemistry, potentially leading to the creation of new drugs.
7. Synthesized as a building block for organic compounds
Explanation
The compound can be used as a starting material in the synthesis of various organic compounds, due to its unique structure and properties.
Check Digit Verification of cas no
The CAS Registry Mumber 105018-99-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,5,0,1 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 105018-99:
(8*1)+(7*0)+(6*5)+(5*0)+(4*1)+(3*8)+(2*9)+(1*9)=93
93 % 10 = 3
So 105018-99-3 is a valid CAS Registry Number.
105018-99-3Relevant academic research and scientific papers
Highly efficient acetalization of carbonyl compounds catalyzed by anilin-aldehyde resin salts
Tanemura, Kiyoshi,Suzuki, Tsuneo
supporting information, p. 797 - 799 (2015/06/22)
A mild procedures for the syntheses of ethylene acetals and dimethyl acetals from the corresponding aldehydes and ketones catalyzed by 1mol% of anilinealdehyde resin salts are described. This method is also useful for the synthesis of dimethyl acetals of diaryl ketones.
Catalytic asymmetric epoxidation
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Page column 33, (2010/01/30)
A compound and method for producing an enantiomerically enriched epoxide from an olefin using a chiral ketone and an oxidizing agent is disclosed.
An efficient procedure for the preparation of cyclic ketals and thioketals catalyzed by zirconium sulfophenyl phosphonate
Curini,Epifano,Marcotullio,Rosati
, p. 1182 - 1184 (2007/10/03)
A convenient method for the preparation of cyclic ketals and thioketals using zirconium sulfophenyl phosphonate as catalyst is described.
Distannoxane-catalyzed acetilization of carbonyls
Otera, Junzo,Dan-oh, Nobuhisa,Nozaki, Hitosi
, p. 1449 - 1456 (2007/10/02)
1,3-Disubstituted tetrabutyldistannoxanes catalyze acetilization of carbonyl compounds under mild conditions. Thorough investigations of factors influencing this reaction are given. A variety of synthetically useful carbonyl compounds are efficiently converted to acetals. In particular, acetilization of cyclic α,β-unsaturated ketones is readily achieved which have met with only limited success so far.
