93780-84-8 Usage
Uses
Used in Pharmaceutical Industry:
(5aR,8aR,9R)-9-(4-hydroxy-3,5-dimethoxy-phenyl)-5a,6,8a,9-tetrahydroisobenzofurano[5,6-f][1,3]benzodioxole-5,8-dione is used as a potential therapeutic agent for various applications due to its complex structure and the presence of aromatic rings, hydroxy group, and methoxy groups. These structural features may allow the molecule to interact with biological targets, making it a candidate for the development of new drugs.
Used in Chemical Research:
In the field of chemical research, (5aR,8aR,9R)-9-(4-hydroxy-3,5-dimethoxy-phenyl)-5a,6,8a,9-tetrahydroisobenzofurano[5,6-f][1,3]benzodioxole-5,8-dione can be used as a starting material or a model compound for studying the synthesis and reactions of complex organic molecules with fused-ring systems. Its unique structure and stereochemistry make it an interesting subject for exploring new synthetic pathways and understanding the reactivity of similar compounds.
Used in Material Science:
The complex structure and potential for various interactions due to the presence of aromatic rings, hydroxy group, and methoxy groups in (5aR,8aR,9R)-9-(4-hydroxy-3,5-dimethoxy-phenyl)-5a,6,8a,9-tetrahydroisobenzofurano[5,6-f][1,3]benzodioxole-5,8-dione may also find applications in material science. It could be investigated for its potential use in the development of new materials with specific properties, such as improved stability, reactivity, or selectivity in various chemical processes.
Check Digit Verification of cas no
The CAS Registry Mumber 93780-84-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,7,8 and 0 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 93780-84:
(7*9)+(6*3)+(5*7)+(4*8)+(3*0)+(2*8)+(1*4)=168
168 % 10 = 8
So 93780-84-8 is a valid CAS Registry Number.
93780-84-8Relevant academic research and scientific papers
A novel enzymatic dehydrogenation of podophyllotoxin congeners by yeast cells
Kamal, Ahmed,Damayanthi
, p. 657 - 662 (2007/10/03)
The biotransformation of aryltetralin lignans to arylnaphthalene lignans in presence of yeast is described. Podophyllotoxone, an oxidation product of podophyllotoxin on incubation with yeast from different sources produced dehydropodophyllotoxin, an important representative of arylnaphthalene lignans.
ARYLTETRALIN LIGNANS FROM PODOPHYLLUM HEXANDRUM AND PODOPHYLLUM PELTATUM
Jackson, David E.,Dewick, Paul M.
, p. 1147 - 1152 (2007/10/02)
Roots of Podophyllum hexandrum and P. peltatum contain the same range of ten aryltetralin lignans: podophyllotoxin, 4'-demethylpodophyllotoxin, α-peltatin, β-peltatin, desoxypodophyllotoxin, podophyllotoxone, isopicropodophyllone, 4'-demetyldesoxypodophyllotoxin, 4'-demethylpodophyllotoxone and 4'-demethylisopicropodophyllone, although the relative proportions are markedly different.The latter two compounds are previously unreported natural products, but 4'-demethylisopicropodophyllone may well be an artefact resulting from epimerization of 4'-demethylpodophyllotoxone.The peltatins have not previously been isolated from P. hexandrum.Key Word Index - Podophyllum hexandrum; P. peltatum; Podophyllaceae; aryltetralin; lignans; podophyllotoxin.
