527-90-2 Usage
Uses
Used in Chemical Synthesis:
(1aR,7aα,7bβ)-Decahydro-1,1,3aβ,7-tetramethyl-1H-cyclopropa[a]naphthalen-7α-ol is used as an intermediate in chemical synthesis for the production of various compounds. Its unique structure allows it to serve as a building block for the creation of new molecules with specific properties.
Used in Pharmaceutical Development:
In the pharmaceutical industry, (1aR,7aα,7bβ)-Decahydro-1,1,3aβ,7-tetramethyl-1H-cyclopropa[a]naphthalen-7α-ol is used as a potential candidate for drug development. Its chemical features may contribute to the design of new drugs with therapeutic applications, pending further research into its pharmacological properties and efficacy.
Used in Material Science:
(1aR,7aα,7bβ)-Decahydro-1,1,3aβ,7-tetramethyl-1H-cyclopropa[a]naphthalen-7α-ol may also find applications in material science, where its structural attributes could be leveraged to develop new materials with specialized characteristics for use in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 527-90-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 5,2 and 7 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 527-90:
(5*5)+(4*2)+(3*7)+(2*9)+(1*0)=72
72 % 10 = 2
So 527-90-2 is a valid CAS Registry Number.
527-90-2Relevant academic research and scientific papers
Rearrangement reactions of aromadendrane derivatives. The synthesis of (+)-maaliol, starting from natural (+)-aromadendrene-IV
Gijsen, Harrie J. M.,Wijnberg, Joannes B. P. A.,Van Ravenswaay, Connie,De Groot, Aede
, p. 4733 - 4744 (2007/10/02)
Starting from the hydroazulene α-ketol 6, which can easily be prepared from (+)-aromadendrene (1); two different routes to hydronaphthalene compounds with a maaliane skeleton have been developed, both proceeding in high overall yield. The first route leads to cis-fused maaliane derivatives; the second one offers access to trans-fused maaliane sesquiterpenes, as demonstrated in this paper in the synthesis of (+)-maaliol (5).
