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(+)-7-epi-α-cyperone is a naturally occurring sesquiterpene compound, which belongs to the class of organic compounds known as cyclohexenones. It is an enantiomer of α-cyperone, featuring a seven-membered ring structure with a hydroxyl group and a methyl group attached to the carbon atoms. This chiral molecule is found in the essential oils of certain plants, particularly in the Cyperaceae family, and is known for its potential biological activities, such as antimicrobial and insecticidal properties. The specific configuration of the molecule, with the hydroxyl group on the upper side of the ring when viewed from a particular perspective, distinguishes it from its enantiomer. Research on compounds like (+)-7-epi-α-cyperone is important for understanding their role in plant defense mechanisms and for potential applications in agriculture and medicine.

547-26-2

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547-26-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 547-26-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,4 and 7 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 547-26:
(5*5)+(4*4)+(3*7)+(2*2)+(1*6)=72
72 % 10 = 2
So 547-26-2 is a valid CAS Registry Number.

547-26-2Relevant academic research and scientific papers

Practical Routes to Two Functionalized Decalones for the Synthesis of Quassinoids

Ziegler, Frederic E.,Hwang, Ki-Jun,Kadow, John F.,Klein, Scott I.,Pati, Uttam K.,Wang, Tein-Fu

, p. 4573 - 4579 (2007/10/02)

The chiral keto alcohol 6a was prepared from (S)-(+)-carvone.Because two steps in this process gave only modest yields of isolated materials, an alternative route was developed.Racemic keto alcohol 6b was prepared from enedione rac-13a by a more efficient process.

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