102130-90-5 Usage
Description
(1S)-7-Isopropylidene-1,2,3,3aα,4,5,6,7,8,8aβ-decahydro-1β-hydroxy-1-methyl-4-methyleneazulen-6-one is a complex organic compound derived from azulen, a bicyclic sesquiterpene commonly found in essential oils. This specific derivative features a ketone with a hydroxyl group and a methyl group attached to the azulen ring, which may confer potential medicinal or therapeutic properties. Its anti-inflammatory and antioxidant characteristics, inherited from azulen, suggest possible applications in various fields, although further research is required to explore its full potential.
Uses
Used in Pharmaceutical Industry:
(1S)-7-Isopropylidene-1,2,3,3aα,4,5,6,7,8,8aβ-decahydro-1β-hydroxy-1-methyl-4-methyleneazulen-6-one is used as a potential therapeutic agent for its anti-inflammatory and antioxidant properties, which may be beneficial in the development of treatments for various conditions.
Used in Cosmetic Industry:
In the cosmetic industry, this compound may be utilized for its anti-inflammatory and antioxidant effects, potentially contributing to skincare products that aim to reduce inflammation and protect the skin from oxidative stress.
Used in Nutraceutical Industry:
(1S)-7-Isopropylidene-1,2,3,3aα,4,5,6,7,8,8aβ-decahydro-1β-hydroxy-1-methyl-4-methyleneazulen-6-one could be employed as an ingredient in nutraceutical products, leveraging its potential health benefits for consumers seeking natural alternatives to support their well-being.
Check Digit Verification of cas no
The CAS Registry Mumber 102130-90-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,2,1,3 and 0 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 102130-90:
(8*1)+(7*0)+(6*2)+(5*1)+(4*3)+(3*0)+(2*9)+(1*0)=55
55 % 10 = 5
So 102130-90-5 is a valid CAS Registry Number.
102130-90-5Relevant articles and documents
Structural diversity from the transannular cyclizations of natural germacrone and epoxy derivatives: A theoretical-experimental study
Pérez Morales, M. Carmen,Catalán, Julieta V.,Domingo, Victoriano,Jaraíz, Martín,Herrador, M. Mar,Quílez Del Moral, José F.,L?pez-Pérez, José-Luis,Barrero, Alejandro F.
, p. 6598 - 6612 (2013/06/27)
Treatment of germacrone (1) with different electrophiles, and of its epoxy derivatives germacrone-4,5-epoxide (2), germacrone-1,10-epoxide (3) and isogermacrone-4,5-epoxide (4) with Br?nsted/Lewis acids and Ti III, gives rise to a great structural diversity. Thus, by using a maximum of two steps, the production of more than 40 compounds corresponding to 14 skeletons is described. Computational calculations rationalizing the structural divergence produced are also described. Finally, since some of the compounds generated are bioactive natural sesquiterpenes, the mechanisms of formation of these substances will provide new insights in their biosynthesis. Copyright
