10579-93-8 Usage
Uses
Used in Perfumery and Fragrance Industry:
[1S-(1R,4E,9S)]-4,11,11-trimethyl-8-methylenebicyclo[7.2.0]undec-4-ene is used as a fragrance ingredient for its strong aromatic scent. [1S-(1R,4E,9S)]-4,11,11-trimethyl-8-methylenebicyclo[7.2.0]undec-4-ene's natural occurrence in essential oils and plant extracts makes it a desirable component in the creation of various perfumes and fragrances, adding depth and complexity to the scents.
Used in Pharmaceutical Research:
[1S-(1R,4E,9S)]-4,11,11-trimethyl-8-methylenebicyclo[7.2.0]undec-4-ene is used as a subject of study in pharmaceutical research due to its potential biological activities. [1S-(1R,4E,9S)]-4,11,11-trimethyl-8-methylenebicyclo[7.2.0]undec-4-ene's antimicrobial, anti-inflammatory, and antioxidant properties make it a promising candidate for the development of new drugs and treatments for various conditions.
Used in Essential Oils Industry:
[1S-(1R,4E,9S)]-4,11,11-trimethyl-8-methylenebicyclo[7.2.0]undec-4-ene is used as a key component in the essential oils industry, where it contributes to the unique scents and potential therapeutic properties of various plant-based oils. Its presence in essential oils can be beneficial for aromatherapy and other applications that utilize the natural healing properties of these oils.
Check Digit Verification of cas no
The CAS Registry Mumber 10579-93-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,0,5,7 and 9 respectively; the second part has 2 digits, 9 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 10579-93:
(7*1)+(6*0)+(5*5)+(4*7)+(3*9)+(2*9)+(1*3)=108
108 % 10 = 8
So 10579-93-8 is a valid CAS Registry Number.
InChI:InChI=1/C15H24/c1-11-6-5-7-12(2)13-10-15(3,4)14(13)9-8-11/h6,13-14H,2,5,7-10H2,1,3-4H3/b11-6-/t13-,14-/m0/s1
10579-93-8Relevant academic research and scientific papers
EIGHT NEW XENIA DITERPENOIDS FROM THREE SOFT CORALS OF THE RED SEA
Groweiss, Amiram,Kashman, Yoel
, p. 3385 - 3396 (2007/10/02)
Investigation of the terpenoid content of three soft corals from the Gulf of Eilat (THe Red Sea), Xenia macrospiculata, X. obscuronata and X. lilielae resulted in the isolation of 8 new diterpens.Two of the new compounds belong to the xeniolides (xenialactol-D (10a) and xeniolide-E (13)) and the other six (4,14-diepoxyxeniaphyllene (15), 4,5-epoxyxeniaphyllan-14,15-diol (17), 4,14-diepoxy-xeniaphyllenol-A (21a), xeniaphyllenol-B (23a), xeniaphyllenol-C (24a) and xeniaphyllantriol (25) are new xeniaphyllanes (prenylated caryophyllanes).The structure determination of the various compounds is based on chemical transformations as well as on the 1H and 13C NMR spectra.Several known caryophyllene derivatives have been synthesised for 13C NMR spectra and chemical comparisons.The 13C NMR has proven to be an excellent probe for structural and stereochemical determinations.
