66275-07-8 Usage
Uses
Used in Organic Chemistry:
(3R,5'aR)-5-(3-Furyl)-7'β-methyl-3',5',5'aα,7',8',8'aα-hexahydrospiro[furan-3(2H),6'-[6H]naphtho[1,8-bc]furan]-2,2'(4'H)-dione is used as a building block for the synthesis of other complex organic molecules. Its unique spiro-structure and functional groups make it a valuable component in the development of novel organic compounds.
Used in Medicinal Chemistry:
(3R,5'aR)-5-(3-Furyl)-7'β-methyl-3',5',5'aα,7',8',8'aα-hexahydrospiro[furan-3(2H),6'-[6H]naphtho[1,8-bc]furan]-2,2'(4'H)-dione is used as a potential lead compound in the discovery and development of new drugs. Its unique structure and potential biological activities may contribute to the design of innovative therapeutic agents.
Used in Pharmaceutical Research:
(3R,5'aR)-5-(3-Furyl)-7'β-methyl-3',5',5'aα,7',8',8'aα-hexahydrospiro[furan-3(2H),6'-[6H]naphtho[1,8-bc]furan]-2,2'(4'H)-dione is used as a subject of investigation in pharmaceutical research to explore its potential biological activities and therapeutic applications. Further studies are needed to determine its specific uses and properties in the development of new medications.
Check Digit Verification of cas no
The CAS Registry Mumber 66275-07-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,6,2,7 and 5 respectively; the second part has 2 digits, 0 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 66275-07:
(7*6)+(6*6)+(5*2)+(4*7)+(3*5)+(2*0)+(1*7)=138
138 % 10 = 8
So 66275-07-8 is a valid CAS Registry Number.
66275-07-8Relevant academic research and scientific papers
Lourenco, Ana,De La Torre, Maria C.,Rodriguez, Benjamin
, p. 7305 - 7308 (1991)
Starting from montanin A (3) compound 11 was obtained by opening of the C-20,C-12 γ-lactone (6), oxidation of the C-12 hydroxyl group (9), relactonization to the β,γ-unsaturated γ-lactone (10) via the C-12 enol form, and final selective air oxidation of the α,β,β′-trialkyl furan to the corresponding α,β-unsaturated γ-lactone (11). Compound 11 was identical to isocrotocaudin, to which structure 1 has previously been assigned only on spectroscopic grounds. The above transformation establishes that the previous 8S configuration of isocrotocaudin (1) and its related C-6,C-10 stereoisomer crotocaudin (2) must be corrected to 8R.
