24959-83-9 Usage
Description
(-)-Isosativene, a naturally occurring sesquiterpene, is an organic compound that can be found in certain plants. It is known for its pleasant, woody aroma and has been identified as a component of essential oils from various plant sources. This chemical has demonstrated potential antimicrobial and insecticidal properties, as well as therapeutic effects such as pain relief and anti-inflammatory action. The unique chemical structure and properties of (-)-Isosativene make it a promising candidate for further research and potential applications across different industries.
Uses
Used in Pharmaceutical Industry:
(-)-Isosativene is used as a therapeutic agent for its pain-relieving and anti-inflammatory effects. Its potential to alleviate pain and reduce inflammation makes it a valuable compound for the development of new medications and treatments.
Used in Agricultural Industry:
(-)-Isosativene is used as an antimicrobial and insecticidal agent to protect crops and enhance agricultural productivity. Its natural properties can help control pests and diseases, reducing the need for chemical pesticides.
Used in Perfumery Industry:
(-)-Isosativene is used as a fragrance ingredient for its pleasant, woody aroma. It can be incorporated into perfumes, colognes, and other scented products to provide a unique and appealing scent profile.
Check Digit Verification of cas no
The CAS Registry Mumber 24959-83-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,9,5 and 9 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 24959-83:
(7*2)+(6*4)+(5*9)+(4*5)+(3*9)+(2*8)+(1*3)=149
149 % 10 = 9
So 24959-83-9 is a valid CAS Registry Number.
24959-83-9Relevant articles and documents
STABLE CARBOCATIONS FROM TERPENOIDS.IX. MOLECULAR REARRANGEMENTS OF α-MUROLENE AND α-COPAENE WITH THE FORMATION OF TRICYCLIC COMPOUNDS
Polovinka, M. P.,Mamatyuk, V. I.,Korchagina, D. V.,Sal'nikov, G. E.,Gatilov, Yu. V.,et al.
, p. 863 - 882 (2007/10/02)
Tricyclic compounds were obtained from α-murolene and α-copaene in superacidic media, and this agrees with the scheme for the biogenetic transformations of these substances.It was found that the temperature at which the stable cations are generated from α-murolene has an effect on the ratio of the paths leading to the formation of the bi- and tricyclic ions.The prediction of the most probable paths for the transformation of α-copaene agrees with the actually observed transformation of the stable ions generated from this substance.The preferred direction in the ske letal rearrangements of the investigated compounds depends on the nature of the acid medium.
