25966-79-4 Usage
Uses
Used in Fragrance and Flavoring Applications:
[1aS-(1aalpha,2alpha,4abeta,8aR)]-octahydro-2,4a,8,8-tetramethylcyclopropa[d]naphthalen-3(1H)-one is used as a key ingredient in the perfume industry for its unique scent and ability to enhance the overall fragrance of various products. Its natural origin and complex structure contribute to the creation of distinct and long-lasting scents.
Used in Pharmaceutical Applications:
In the pharmaceutical industry, [1aS-(1aalpha,2alpha,4abeta,8aR)]-octahydro-2,4a,8,8-tetramethylcyclopropa[d]naphthalen-3(1H)-one may be utilized as a starting material for the development of new drugs or as an active ingredient itself. Its structural diversity and biological activity make it a promising candidate for various therapeutic applications.
Used in Agrochemical Applications:
The potential use of [1aS-(1aalpha,2alpha,4abeta,8aR)]-octahydro-2,4a,8,8-tetramethylcyclopropa[d]naphthalen-3(1H)-one in the agrochemical industry lies in its ability to serve as a component in the development of new pesticides, herbicides, or other agricultural chemicals. Its unique properties and natural origin could contribute to the creation of more effective and environmentally friendly products.
Check Digit Verification of cas no
The CAS Registry Mumber 25966-79-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,5,9,6 and 6 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 25966-79:
(7*2)+(6*5)+(5*9)+(4*6)+(3*6)+(2*7)+(1*9)=154
154 % 10 = 4
So 25966-79-4 is a valid CAS Registry Number.
25966-79-4Relevant academic research and scientific papers
Acid-catalyzed rearrangements of (-)-thujopsene
Yarovaya,Polovinka,Korchagina,Gatilov,Bagryanskaya,Shcherbukhin,Shal'ko,Zenkovets,Barkhash
, p. 362 - 374 (2007/10/03)
The transformations of (-)-thujopsene in liquid (HSO3F-SO2FCl) and over solid (TiO2/SO24) superacids, as well as by the action of peroxy acids, were studied. New tricyclic hydrocarbons were isolated.
Terpenoids. X. Natural Autoxidation of Thujopsene
Nagahama, Shizuo,Tazaki, Masato
, p. 4453 - 4454 (2007/10/02)
The natural autoxidation of thujopsene 1 afforded three dimeric peroxides (14, 15, and 16) as the major products. 9α,10-Epoxy-8α-thujopsanol 17 was separated as a minor product besides other known compounds, allylic alcohols 2 and 3, mayurone 7, thujopsane-8α,9α-diol 11, and thujopsan-9-ones 19 and 20.
