65714-69-4 Usage
Uses
Used in Medicinal Chemistry:
(4aR)-2,3,4,4a-Tetrahydro-5,6,8,10-tetrahydroxy-1,1,4a-trimethyl-7-isopropylphenanthren-9(1H)-one is used as a compound in medicinal chemistry for its complex structure and functional groups, which may contribute to the development of new pharmaceutical agents.
Used in Pharmaceuticals:
In the pharmaceutical industry, (4aR)-2,3,4,4a-Tetrahydro-5,6,8,10-tetrahydroxy-1,1,4a-trimethyl-7-isopropylphenanthren-9(1H)-one is used as a potential candidate for drug development due to its unique molecular configuration and functional groups that could be harnessed for therapeutic purposes.
Used in Organic Synthesis:
(4aR)-2,3,4,4a-Tetrahydro-5,6,8,10-tetrahydroxy-1,1,4a-trimethyl-7-isopropylphenanthren-9(1H)-one is utilized in organic synthesis as a building block or intermediate for creating more complex organic molecules, potentially leading to innovative materials or chemical products.
Check Digit Verification of cas no
The CAS Registry Mumber 65714-69-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,7,1 and 4 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 65714-69:
(7*6)+(6*5)+(5*7)+(4*1)+(3*4)+(2*6)+(1*9)=144
144 % 10 = 4
So 65714-69-4 is a valid CAS Registry Number.
InChI:InChI=1/C20H26O5/c1-9(2)10-13(21)11-12(16(24)14(10)22)20(5)8-6-7-19(3,4)18(20)17(25)15(11)23/h9,21-22,24-25H,6-8H2,1-5H3/t20-/m1/s1
65714-69-4Relevant academic research and scientific papers
14-Hydroxytaxodion: Partialsynthese und Reaktionen
Rueedi, Peter,Eugster, Conrad Hans
, p. 2219 - 2226 (2007/10/02)
The hitherto unknown diterpenoid 14-hydroxytaxodione (10a) has been prepared by oxidation of 6β-hydroxyroyleanone.Its solutions exhibit a dynamic structural behaviour (UV./VIS. and NMR.) and lead to an equilibrium mixture of the 11,14- and the 6,12-dioxo forms.By methylation and acetylation the 6,12-dioxo form can be isolated.Chloroform solutions of 14-hydroxytaxodione slowly set up a mixture of coleon V (2a), coleon U (3) and dimeric products (later established as grandidone C, grandidone D and 7-epigrandidone D).Therefore, coleon V (2a) owing to its strong intramolecular H-bond is more stable than 7,14-dihydroxytaxodione (2b).
