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4-methyl-4-(3-oxobutyl)cyclohex-2-en-1-one is a complex organic compound with the molecular formula C12H18O2. It is a derivative of cyclohexenone, featuring a methyl group at the 4-position and a 3-oxobutyl group attached to the same carbon. The 3-oxobutyl group consists of a butyl chain with a carbonyl group at the third carbon, which contributes to the compound's reactivity and properties. This chemical is characterized by its unique structure, which includes a cyclohexene ring and a ketone functional group, making it a potentially useful intermediate in the synthesis of various pharmaceuticals and other organic compounds. Its specific applications and properties would depend on the context in which it is used, such as in chemical research or industrial processes.

5259-53-0

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5259-53-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5259-53-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,5 and 9 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5259-53:
(6*5)+(5*2)+(4*5)+(3*9)+(2*5)+(1*3)=100
100 % 10 = 0
So 5259-53-0 is a valid CAS Registry Number.

5259-53-0Downstream Products

5259-53-0Relevant academic research and scientific papers

Aldol condensation versus conjugate addition: Intramolecular cyclization using a combination of Lewis acid and 1,2-diol

Yamada,Suemune

, p. 1171 - 1175 (2007/10/03)

The reactivity of 3-substituted 4-methyl-4-(3-oxobutyl)-2-cyclohexen-1-ones (1) in the presence of a combination of a Lewis acid and a 1,2-diol was studied. The results suggest several factors that influence 6-membered ring formation, including two types of intramolecular aldol reaction and intramolecular 1,4-addition, due to the C3-substituent, Lewis acid, and the presence of diol. In this study, novel methodology to prepare two types of decalin skeleton could be developed.

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