158761-01-4 Usage
Uses
Used in Pharmaceutical Industry:
(3S,6aS,9S,10R,10aR)-4-formyl-3,9-dihydroxy-7,7-dimethyl-1-oxo-3,3a,6,6a,7,8,9,10-octahydronaphtho[1,8a-c]furan-10-yl 2-hydroxydecanoate is used as a potential pharmaceutical candidate for its possible biological activity. (3S,6aS,9S,10R,10aR)-4-formyl-3,9-dihydroxy-7,7-dimethyl-1-oxo-3,3a,6,6a,7,8,9,10-octahydronaphtho[1,8a-c]furan-10-yl 2-hydroxydecanoate's unique structure, including the formyl, hydroxyl, and ester groups, may allow it to interact with biological targets, making it a candidate for drug development.
Used in Organic Synthesis:
In the field of organic chemistry, (3S,6aS,9S,10R,10aR)-4-formyl-3,9-dihydroxy-7,7-dimethyl-1-oxo-3,3a,6,6a,7,8,9,10-octahydronaphtho[1,8a-c]furan-10-yl 2-hydroxydecanoate is used as a synthetic intermediate. Its reactivity and functional groups can be leveraged in the synthesis of more complex molecules, potentially leading to the development of new compounds with specific applications in various industries.
Used in Chemical Research:
(3S,6aS,9S,10R,10aR)-4-formyl-3,9-dihydroxy-7,7-dimethyl-1-oxo-3,3a,6,6a,7,8,9,10-octahydronaphtho[1,8a-c]furan-10-yl 2-hydroxydecanoate is utilized in chemical research to study the properties and reactions of complex organic molecules. Understanding its reactivity and interactions can contribute to the advancement of organic chemistry and the discovery of new synthetic pathways.
Check Digit Verification of cas no
The CAS Registry Mumber 158761-01-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,8,7,6 and 1 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 158761-01:
(8*1)+(7*5)+(6*8)+(5*7)+(4*6)+(3*1)+(2*0)+(1*1)=154
154 % 10 = 4
So 158761-01-4 is a valid CAS Registry Number.
158761-01-4Relevant academic research and scientific papers
Total synthesis of mniopetals A, B, C and D
Weihrather, Joachim,Jauch, Johann
, p. 1410 - 1414 (2013/07/26)
A total synthesis of the mniopetals A, B, C and D is described. Key steps are a Sharpless asymmetric dihydroxylation and a selective esterification of an equatorial hydroxy group vicinal to an axial hydroxy function. Georg Thieme Verlag Stuttgart · New York.
