155485-76-0 Usage
Uses
Used in Pharmaceutical Industry:
3,6-Caryolanediol is used as a potential medicinal compound for its possible therapeutic applications. Its origin from a plant species used in traditional medicine indicates that it may possess bioactive properties that could be harnessed for the development of new drugs or treatments.
Used in Research and Development:
3,6-Caryolanediol is used as a subject of scientific research to further understand its chemical properties, potential medicinal uses, and any associated risks. Ongoing studies aim to uncover its full potential and establish its role in the field of medicine and healthcare.
Used in Traditional Medicine:
3,6-Caryolanediol is used in traditional medicine practices, where the liverwort plant of the Radula genus has been employed for its supposed healing properties. 3,6-Caryolanediol may contribute to the overall efficacy of these traditional remedies, although more research is needed to validate its specific contributions and safety.
Check Digit Verification of cas no
The CAS Registry Mumber 155485-76-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,5,5,4,8 and 5 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 155485-76:
(8*1)+(7*5)+(6*5)+(5*4)+(4*8)+(3*5)+(2*7)+(1*6)=160
160 % 10 = 0
So 155485-76-0 is a valid CAS Registry Number.
155485-76-0Relevant academic research and scientific papers
MOLECULAR REARRANGEMENTS OF CARYOPHYLLENE AND ISOCARYOPHYLLENE 4,5-EPOXIDES IN SUPERACIDIC MEDIA
Nisnevich, G. A.,Korchagina, D. V.,Makal'skii, V. I.,Dubovenko, Zh. V.,Barkhash, V. A.
, p. 441 - 453 (2007/10/02)
Enantiomeric stable carbocations were generated from the epimeric pair of optically active isocaryophyllene 4β,5β- and 4α,5α-epoxides in the superacid.The subsequent molecular rearrangement path is determined by participation of the ? and ? bonds in opening of the epoxide ring.For the case of caryophyllene 4β,5α- and 4α,5β-epoxides it was shown that rearrangement to compounds with the clovane or caryolane skeleton respectively is possible.The rearrangement of a compound of the caryophyllane type to compounds of the selinane group was realized for the first time.For the case of caryophyllene 4β,5α-epoxide it was shown that the generation temperature of the ions has a significant effect on the preferred position of the cationic center.
