81842-08-2 Usage
Chemical structure
1,4-Dioxaspiro[4.5]dec-6-ene, 8-methyl-
Explanation
This compound has a unique 1,4-dioxaspiro ring system, which is a fused ring structure containing two oxygen atoms and a six-membered carbon ring. The 8-methyl group is attached to the ring, indicating the presence of a methyl group (CH3) at the 8th position.
Explanation
A spiroketone is a type of organic compound that contains a spiro ring system and a ketone functional group. In this case, the spiro ring system is a 1,4-dioxaspiro[4.5]decane, and the ketone group is part of the dec-6-ene structure.
Explanation
1,4-Dioxaspiro[4.5]dec-6-ene, 8-methylis used as a building block for creating more complex molecules in organic synthesis and chemical research. It is also used in the fragrance industry due to its aromatic properties and has potential applications in the pharmaceutical industry.
Explanation
The unique 1,4-dioxaspiro ring system and the presence of a methyl group make this compound a valuable tool for researchers in the fields of chemistry and pharmaceuticals. Its structure can be used to develop new molecules with specific properties and potential applications.
Type of compound
Spiroketone
Applications
Organic synthesis, chemical research, fragrance ingredient, pharmaceutical industry
Unique structure
Valuable tool in chemical and pharmaceutical research and development
Check Digit Verification of cas no
The CAS Registry Mumber 81842-08-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,8,4 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 81842-08:
(7*8)+(6*1)+(5*8)+(4*4)+(3*2)+(2*0)+(1*8)=132
132 % 10 = 2
So 81842-08-2 is a valid CAS Registry Number.
81842-08-2Relevant articles and documents
A NEW SYNTHON FOR THE REGIOSPECIFIC γ-ALKYLATION OF 2-CYCLOHEXENONES. APPLICATION TO THE SYNTHESIS OF ZINGIBERENOL AND OXYGENATED BICYCLONONANES
Paquette, Leo A.,Kinney, William A.
, p. 131 - 134 (2007/10/02)
The regiospecific γ-alkylation of γ-sulfonylcyclohexenone ketals is described and applied to various synthetic objectives.