87206-33-5 Usage
Description
(1aR,4R,4aS,7R,7aS,9aR)-4,7,9a-trimethyldecahydro-3H-oxireno[7,8]naphtho[8a,1-b]furan-3-one is a bicyclic triterpenoid with a complex and specific structure. It has a molecular formula of C15H24O2 and a molecular weight of 236.35 g/mol. As a member of the oxirane class of compounds, it features a unique carbon skeleton and multiple stereocenters, making it of interest to organic chemists. The presence of various functional groups in its structure suggests potential biological activity and pharmaceutical applications, which may be explored for its potential medicinal properties or as a starting material for the synthesis of other organic compounds.
Uses
Used in Pharmaceutical Industry:
(1aR,4R,4aS,7R,7aS,9aR)-4,7,9a-trimethyldecahydro-3H-oxireno[7,8]naphtho[8a,1-b]furan-3-one is used as a potential pharmaceutical candidate for its possible biological activity due to its unique structure and functional groups. It may be studied for its potential medicinal properties, such as treating specific diseases or conditions.
Used in Organic Synthesis:
(1aR,4R,4aS,7R,7aS,9aR)-4,7,9a-trimethyldecahydro-3H-oxireno[7,8]naphtho[8a,1-b]furan-3-one is used as a starting material in organic synthesis for the development of other organic compounds. Its unique carbon skeleton and functional groups make it a valuable component in creating new molecules with potential applications in various fields, such as materials science, pharmaceuticals, or agrochemicals.
Check Digit Verification of cas no
The CAS Registry Mumber 87206-33-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,2,0 and 6 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 87206-33:
(7*8)+(6*7)+(5*2)+(4*0)+(3*6)+(2*3)+(1*3)=135
135 % 10 = 5
So 87206-33-5 is a valid CAS Registry Number.
87206-33-5Relevant articles and documents
The mechanism of the spontaneous autoxidation of dihydroartemisinic acid
Sy, Lai-King,Brown, Geoffrey D
, p. 897 - 908 (2007/10/03)
Dihydroartemisinic acid undergoes slow spontaneous autoxidation to artemisinin and other natural products, which have been reported from the medicinal plant Artemisia annua. The mechanism of this complex transformation is shown to involve four steps: (i) initial reaction of the Δ4.5-double bond of dihydroartemisinic acid with molecular oxygen, (ii) Hock cleavage of the resulting tertiary allylic hydroperoxide; (iii) oxygenation of the enol product from Hock cleavage; and (iv) cyclization of the resulting vicinal hydroperoxyl-aldehyde to the 1,2,4-trioxane system of artemisinin.