506441-55-0 Usage
Uses
Used in Organic Chemistry:
2,5,7-Metheno-1H-cyclopenta[a]pentalen-3-ol,decahydro-,(2S,3S,3aS,3bS,5S,6aR,7R,7aR,8R)-(9CI) is used as a building block or intermediate in the synthesis of more complex organic compounds due to its unique structure and functional groups.
Used in Pharmacology:
2,5,7-Metheno-1H-cyclopenta[a]pentalen-3-ol,decahydro-,(2S,3S,3aS,3bS,5S,6aR,7R,7aR,8R)-(9CI) is used as a potential pharmaceutical candidate for the development of new drugs, given its unique structure and the presence of a hydroxyl group, which can be further modified or functionalized for specific therapeutic applications.
Used in Material Science:
2,5,7-Metheno-1H-cyclopenta[a]pentalen-3-ol,decahydro-,(2S,3S,3aS,3bS,5S,6aR,7R,7aR,8R)-(9CI) is used in the development of new materials with unique properties, such as polymers, coatings, or composites, leveraging its complex structure and functional groups for specific applications.
Check Digit Verification of cas no
The CAS Registry Mumber 506441-55-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 5,0,6,4,4 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 506441-55:
(8*5)+(7*0)+(6*6)+(5*4)+(4*4)+(3*1)+(2*5)+(1*5)=130
130 % 10 = 0
So 506441-55-0 is a valid CAS Registry Number.
506441-55-0Relevant academic research and scientific papers
Asymmetric synthesis of half-cage alcohol compounds
Alifantes, Joao,Nichele, Aline G.,Costa, Valentim E.U.
, p. 2019 - 2024 (2007/10/03)
To obtain enantiopure pentacyclic chlorinated and dechlorinated alcohols, we evaluated various synthetic routes. Enantiopure acetate (-)-5 (ee >95%) was obtained from an enantioselective inversion of a stereogenic center of the pentacyclic acetate (+)-4 in an acidic medium. Conversely, enantiopure alcohols (+)-11 and (+)-15 were obtained by the kinetic resolution of alcohol (±)-11 by transesterification using lipase from Candida rugosa. It was verified that the lipase recognized alcohol (±)-11, producing the alcohol (+)-11 (ee >98%) and acetate (-)-13 (ee >99%) with a high degree of enantioselectivity (E >100) and a conversion of 50% after only 1 h.
