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Podocarpan-14-one is a naturally occurring organic compound belonging to the podocarpanes class of diterpenes, which are derived from the resin of Podocarpus macrophyllus, a coniferous tree. This chemical is characterized by a unique carbon skeleton with 14 carbon atoms and a ketone functional group at the 14th position. It exhibits various biological activities, such as anti-inflammatory, antitumor, and antimicrobial properties, making it a subject of interest in pharmaceutical research. Podocarpan-14-one's structure and potential applications in drug development highlight its significance in the field of natural products chemistry.

5720-73-0

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5720-73-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5720-73-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,7,2 and 0 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 5720-73:
(6*5)+(5*7)+(4*2)+(3*0)+(2*7)+(1*3)=90
90 % 10 = 0
So 5720-73-0 is a valid CAS Registry Number.

5720-73-0Relevant academic research and scientific papers

Synthesis and mass spectral data of four potential biomarkers related to the C19 tricyclanes found in Australian oils and puget sound sediments

Kaufman

, p. 1205 - 1221 (1995)

The synthesis of four potential biomarkers, 13α-, 13β-, 14α- and 14β-ethyl-8β(H)-podocarpane is reported. GC-MS comparison with an Australian oil C19 tricyclane and the mass spectra of two Puget Sound C19-terpanes evidenced non-identity of the synthetic compounds with the natural products; thus, proposed structures should be revised.

Total Synthesis of the Labdane Diterpenes Galanal A and B from Geraniol

Lin, Shih-Che,Chein, Rong-Jie

, p. 1575 - 1583 (2017/02/10)

The first total synthesis of galanal A and B has been achieved from naturally occurring geraniol. Key steps in this synthesis are the use of a Lewis acid assisted chiral Br?nsted acid (chiral LBA) mediated cationic polyene cyclization and a titanocene-mediated radical cyclization for the asymmetric assembly of the "AB" ring and the construction of the all-carbon quaternary center at the junction of the "BC" ring, respectively.

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