21284-22-0 Usage
Uses
Used in Antioxidant Applications:
(-)-Cubenol is used as an antioxidant agent for its ability to neutralize free radicals and protect cells from oxidative damage. This property makes it a potential candidate for use in the development of health supplements and skincare products.
Used in Antimicrobial Applications:
(-)-Cubenol is used as an antimicrobial agent for its ability to inhibit the growth of bacteria and other microorganisms. This characteristic makes it suitable for use in the formulation of natural preservatives and disinfectants.
Used in Aromatherapy:
(-)-Cubenol is used as a fragrance component in aromatherapy for its pleasant aroma and potential mood-enhancing properties. Its unique scent can contribute to creating a relaxing and soothing atmosphere.
Used in Flavor and Fragrance Industry:
(-)-Cubenol is used as a flavor and fragrance ingredient in the food and cosmetics industries due to its distinctive aroma. It can be used to enhance the taste and smell of various products, such as beverages, confectionery, and perfumes.
Used in Essential Oils:
(-)-Cubenol is used as a major component in essential oils isolated from plants like Artemisia absinthium, Artemisia santonicum, and Artemisia spicigera. These essential oils can be used in various applications, such as aromatherapy, cosmetics, and pharmaceuticals, taking advantage of the antioxidant and antimicrobial properties of (-)-cubenol.
Used in Biological Studies:
(-)-Cubenol is used in biological studies for its antioxidant and antimicrobial activity, as well as for comparative analysis of essential oils and oleoresins from different plant sources, such as cinnamon leaf and bark. This research can help in understanding the therapeutic potential of (-)-cubenol and its applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 21284-22-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,2,8 and 4 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 21284-22:
(7*2)+(6*1)+(5*2)+(4*8)+(3*4)+(2*2)+(1*2)=80
80 % 10 = 0
So 21284-22-0 is a valid CAS Registry Number.
InChI:InChI=1/C15H26O/c1-10(2)13-6-5-12(4)15(16)8-7-11(3)9-14(13)15/h9-10,12-14,16H,5-8H2,1-4H3/t12-,13+,14+,15-/m1/s1
21284-22-0Relevant academic research and scientific papers
Thermal Rearrangement of Bicyclogermacrane-1,8-dione. Synthesis of Humulenedione and (-)-Cubenol, Starting from Natural (+)-Aromadendrene - V
Gijsen, Harrie J. M.,Wijnberg, Joannes B. P. A.,Groot, Aede de
, p. 4745 - 4754 (2007/10/02)
Treatment of a distillation tail of Eucalyptus globulus, containing mainly (+)-aromadendrene (1) and (-)-alloaromadendrene (2), with K/Al2O3 gives a quantitative conversion of 1 and 2 into isoledene (4).Oxidative cleavage of the central double bond in 4 produces (+)-bicyclogermacrane-1,8-dione (5).Thermal rearrangement of 5 gives via a homo hydrogen shift at relatively low temperature the humulenedione 6, and at high temperature (FVP) the products 9 and 10 both with a cadinane skeleton.The naturally occurring humulenedione (7) and (-)-cubenol (17) can be synthesized starting from 6 and 9, respectively. - Key Words: sesquiterpene, flash vacuum pyrolysis, homo hydrogen shift, humulane, cadinane
Total Synthesis of (+/-)-Epicubenol
Cane, David E.,Tandon, Manish
, p. 5351 - 5354 (2007/10/02)
The sesquiterpenoid microbial metabolite (+/-)-epicubenol (1) has been synthesized in 8 steps from readily available diene aldehyde (7) using an intramolecular Diels-Alder reaction.
Epicubebol and Related Sesquiterpenoids from the Brown Alga Dictyopteris divaricata
Suzuki, Minoru,Kowata, Nobuhiko,Kurosawa, Etsuro
, p. 2366 - 2368 (2007/10/02)
Epicubebol has been isolated from the methanol extracts of the brown alga Dictyopteris divaricata as the major constituent.Cadinane-type sesquiterpenes, cubebenes, δ-cadinene, cubenol, and epicubenol, as well as two sesquiterpene methyl ethers as minor constituents have also been obtained from the extracts.
