3242-08-8 Usage
Explanation
The compound consists of 17 carbon atoms and 28 hydrogen atoms.
Explanation
The compound forms a closed carbon ring, with carbon atoms bonded to each other in a cyclic arrangement.
Explanation
The presence of these groups contributes to the compound's structural complexity and chemical reactivity.
Explanation
The compound has several methyl and vinyl groups attached to the main cyclic structure, making its structure more complex.
Explanation
The presence of reactive groups like vinyl and methyl can lead to various chemical reactions, making the compound useful in research and industrial applications.
Explanation
Due to its unique structure and reactivity, the compound may be employed in specific research or industrial processes.
Explanation
The compound should be handled with care, as its complex structure and reactivity may pose risks in certain situations.
Structure
Cyclic hydrocarbon
Functional groups
Methyl, vinyl, and cyclohexane groups
Complexity
Multiple substituents
Reactivity
Potential for chemical reactions
Applications
Research and industrial uses
Safety precautions
Potentially hazardous
Check Digit Verification of cas no
The CAS Registry Mumber 3242-08-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,2,4 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 3242-08:
(6*3)+(5*2)+(4*4)+(3*2)+(2*0)+(1*8)=58
58 % 10 = 8
So 3242-08-8 is a valid CAS Registry Number.
InChI:InChI=1/C15H24/c1-7-15(6)9-8-13(11(2)3)10-14(15)12(4)5/h7,14H,1,4,8-10H2,2-3,5-6H3
3242-08-8Relevant academic research and scientific papers
Efficient synthesis of the anticancer β-elemene and other bioactive elemanes from sustainable germacrone
Barrero, Alejandro F.,Herrador, M. Mar,Quilez Del Moral, Jose F.,Arteaga, Pilar,Meine, Niklas,Perez-Morales, M. Carmen,Catalan, Julieta V.
, p. 1118 - 1125 (2011/04/15)
Highly efficient preparations of anticancer β-elemene and other bioactive elemanes were carried out using the natural product germacrone as a renewable starting material. The syntheses were achieved in only 3-5 steps with excellent overall yields (43-54%). An enantioselective approach to these molecules is also described