16641-47-7 Usage
Uses
Used in Traditional Medicine:
(±)-11-Selinen-4α-ol is used as a traditional medicinal ingredient for its potential therapeutic properties, including anti-inflammatory and antimicrobial activities, which can contribute to the treatment and management of various health conditions.
Used in Fragrances:
(±)-11-Selinen-4α-ol is used as a fragrance ingredient for its pleasant aroma, adding a natural scent to perfumes, cosmetics, and other scented products.
Used in Therapeutic Products:
(±)-11-Selinen-4α-ol is used as an active ingredient in therapeutic products for its anti-inflammatory and antimicrobial properties, potentially valuable in the development of new treatments for various conditions.
Used in Cosmetic Products:
(±)-11-Selinen-4α-ol is used as a key component in cosmetic products, leveraging its anti-inflammatory and antimicrobial properties to improve skin health and provide soothing effects.
Used in Pharmaceutical Research:
(±)-11-Selinen-4α-ol is used as a subject of pharmaceutical research for its potential to contribute to the development of new drugs and therapies, particularly in the areas of inflammation and infection management.
Check Digit Verification of cas no
The CAS Registry Mumber 16641-47-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,6,6,4 and 1 respectively; the second part has 2 digits, 4 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 16641-47:
(7*1)+(6*6)+(5*6)+(4*4)+(3*1)+(2*4)+(1*7)=107
107 % 10 = 7
So 16641-47-7 is a valid CAS Registry Number.
InChI:InChI=1/C15H26O/c1-11(2)12-6-9-14(3)7-5-8-15(4,16)13(14)10-12/h12-13,16H,1,5-10H2,2-4H3/t12-,13-,14-,15-/m1/s1
16641-47-7Relevant academic research and scientific papers
Absolute configuration of helminthogermacrene
Adio, Adewale Martins,Paul, Claudia,Tesso, Hailemichael,Kloth, Petra,Koenig, Wilfried A.
, p. 1631 - 1635 (2007/10/03)
The absolute configuration of the sesquiterpene hydrocarbon helminthogermacrene is established. Helminthogermacrene is an (E,Z)-configurational isomer of germacrene A and thus undergoes similar transformations forming elemenes via Cope rearrangement and yielding bicyclic systems via acid catalyzed reactions. The reaction products are investigated using enantioselective GC and extensive NMR measurements (1H-; 1H1H-COSY; HSQC; HMBC and NOE-experiments). In addition, NMR data of related compounds isolated during the course of this investigation not yet reported in literature are given.
