87480-01-1 Usage
Uses
Used in Pharmaceutical Research:
(3aR,5aS,6S,8aS,8bS)-10,10-dimethyloctahydro-6,8b-ethanocyclopenta[de]isochromene-1,4-dione is used as a subject of study in pharmaceutical research for its potential biological activity and structural features. Its unique molecular configuration and chiral centers may offer insights into the development of new drugs and therapies.
Used in Chemical Synthesis:
In the field of chemical synthesis, (3aR,5aS,6S,8aS,8bS)-10,10-dimethyloctahydro-6,8b-ethanocyclopenta[de]isochromene-1,4-dione may be utilized as a starting material or intermediate in the synthesis of other complex organic compounds. Its unique structure and functional groups could be valuable in creating new molecules with specific properties and applications.
Used in Material Science:
(3aR,5aS,6S,8aS,8bS)-10,10-dimethyloctahydro-6,8b-ethanocyclopenta[de]isochromene-1,4-dione could also be explored in material science for its potential use in the development of new materials with unique properties. Its cyclic structure and chiral centers may contribute to the creation of materials with specific characteristics, such as improved stability or selectivity in chemical reactions.
Note: The specific applications and uses mentioned above are speculative and would require further research and development to confirm their feasibility and effectiveness.
Check Digit Verification of cas no
The CAS Registry Mumber 87480-01-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,4,8 and 0 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 87480-01:
(7*8)+(6*7)+(5*4)+(4*8)+(3*0)+(2*0)+(1*1)=151
151 % 10 = 1
So 87480-01-1 is a valid CAS Registry Number.
87480-01-1Relevant academic research and scientific papers
THE BIOSYNTHESIS OF QUADRONE AND TERRECYCLIC ACID
Cane, David E.,Whittle, Yvonne G.,Liang, Tzyy-Chyau
, p. 1119 - 1122 (2007/10/02)
Feedings of - and acetate to Aspergillus terreus gave quadrone and terrecyclic acid which were analyzed by 13C NMR.The pattern of 13C-enrichments and couplings is consistent with the formation of 1 and 2 by cyclization of farnesyl pyrophosphate.
The Total Synthesis of dl-Quadrone
Danishefsky, Samuel,Vaughan, Kenward,Gadwood, Robert,Tsuzuki, Kazuo
, p. 4136 - 4141 (2007/10/02)
A regio- and stereospecific total synthesis of dl-quadrone (1) is described.The synthesis, which starts with 4,4-dimethylcyclopent-2-en-1-one (5), is accomplished in 19 steps in 3.1percent yield.The key intermediates are the enone ester 4, the iodo ketal 15, the tricyclic keto ester 16, and the hydroxymethyl keto acid 22.The latter as well as the seco acid 2 afford quadrone upon thermolysis.
