59086-93-0 Usage
Uses
Used in Pharmaceutical Industry:
3,3-Dimethyl-6-hydroxy-9,10-dimethoxy-3H-bis[1]benzopyrano[3,4-b:6',5'-e]pyran-7(13H)-one is used as a potential therapeutic agent for its pharmacological activities. The presence of hydroxyl and methoxy groups in its structure may contribute to its interaction with biological targets, making it a candidate for the development of new drugs.
Used in Chemical Research:
3,3-Dimethyl-6-hydroxy-9,10-dimethoxy-3H-bis[1]benzopyrano[3,4-b:6',5'-e]pyran-7(13H)-one serves as a subject of interest in chemical research due to its unique molecular structure and fused ring system. Studying its properties and reactivity can provide insights into the development of new synthetic routes and applications in various fields.
Used in Material Science:
The complex structure of 3,3-Dimethyl-6-hydroxy-9,10-dimethoxy-3H-bis[1]benzopyrano[3,4-b:6',5'-e]pyran-7(13H)-one may offer potential applications in material science, such as in the development of new polymers or materials with specific properties. Its functional groups and fused ring system could contribute to the creation of novel materials with unique characteristics.
Check Digit Verification of cas no
The CAS Registry Mumber 59086-93-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,0,8 and 6 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 59086-93:
(7*5)+(6*9)+(5*0)+(4*8)+(3*6)+(2*9)+(1*3)=160
160 % 10 = 0
So 59086-93-0 is a valid CAS Registry Number.
InChI:InChI=1/C23H20O7/c1-23(2)6-5-11-15(30-23)8-13(24)20-21(25)19-12-7-16(26-3)17(27-4)9-14(12)28-10-18(19)29-22(11)20/h5-9,24H,10H2,1-4H3
59086-93-0Relevant academic research and scientific papers
Synthesis of trans-B/C-Rotenoids: X-Ray and NMR Data for cis- and trans-Forms of Isorotenone
Begley, Michael J.,Crombie, Leslie,Hadi, Hamid bin A.,Josephs, Jonathan L.
, p. 2605 - 2614 (2007/10/02)
Reduction of 6a,12a-didehydrorotenoids with diisobutylaluminium hydride gives clean 1,4-reduction leading to unstable trans-B/C-fusions, not previously known for enolisable rotenoids: they are epimerised to stable cis-forms under acid conditions.Applied initially to isorotenone, the method is extended to trans-B/C-deguelin, α-toxicarol, the 'core' rotenoid structure and the 6aS,12aR,5'R- and 6aR,12aS,5'R-rotenone stereoisomers. 1H and 13C NMR data are compared for the cis- and trans-forms and the geometry and conformations of the isorotenones are compared by X-ray analysis, providing insight into the reasons for the instability of the trans-forms.Reduction of the ridge-tile-like cis-isorotenone by sodium borohydride occurs from one face to give a cis-12α-hydroxy product, whilst the flatter trans-structure is attacked from both faces to give trans-12α- and 12β-hydroxy products.
