4666-84-6 Usage
Description
(1R,8aα)-1,4aβ-Dimethyl-7β-(1-hydroxy-1-methylethyl)decalin-1α-ol is a complex organic compound with a specific molecular structure. It is characterized by its unique arrangement of carbon atoms and functional groups, which contribute to its distinct properties and potential applications.
Uses
Used in Pharmaceutical Industry:
(1R,8aα)-1,4aβ-Dimethyl-7β-(1-hydroxy-1-methylethyl)decalin-1α-ol is used as a pharmaceutical compound for its potential therapeutic effects. Its unique molecular structure allows it to interact with specific biological targets, making it a promising candidate for the development of new drugs.
Used in Cosmetics Industry:
In the cosmetics industry, (1R,8aα)-1,4aβ-Dimethyl-7β-(1-hydroxy-1-methylethyl)decalin-1α-ol is used as an active ingredient for its beneficial properties. Its ability to interact with biopolymers and macromolecules can contribute to the development of innovative skincare products with improved efficacy.
Used in Chemical Research:
(1R,8aα)-1,4aβ-Dimethyl-7β-(1-hydroxy-1-methylethyl)decalin-1α-ol is also used in chemical research as a model compound for studying the properties and behavior of complex organic molecules. This can help researchers gain a deeper understanding of molecular interactions and potentially lead to the discovery of new compounds with specific applications.
Check Digit Verification of cas no
The CAS Registry Mumber 4666-84-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,6,6 and 6 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 4666-84:
(6*4)+(5*6)+(4*6)+(3*6)+(2*8)+(1*4)=116
116 % 10 = 6
So 4666-84-6 is a valid CAS Registry Number.
InChI:InChI=1/C15H28O2/c1-13(2,16)11-6-9-14(3)7-5-8-15(4,17)12(14)10-11/h11-12,16-17H,5-10H2,1-4H3/t11-,12-,14-,15-/m1/s1
4666-84-6Relevant articles and documents
Short and efficient hemisynthesis of α-eudesmol and cryptomeridiol
Tebbaa, Mohamed,El Hakmaoui, Ahmed,Benharref, Ahmed,Akssira, Mohamed
, p. 3769 - 3771 (2011/08/06)
The aerial part of Dittrichia viscosa yielded two sesquiterpenes, isocostic acid (1) and ilicic acid (2), on multigram scale. These acids are appropriate starting materials for short and facile syntheses of α-eudesmol (5) and cryptomeridiol (6), natural products featuring anti-Alzheimer and anti-spasmodic properties. Compounds 5 and 6 were obtained in three steps in overall yields of 70% and 52%, respectively.
SESQUITERPENES FROM LEAVES OF CRYPTOMERIA JAPONICA
Su, Wen-Chiung,Fang, Jim-Min,Cheng, Yu-Shia
, p. 603 - 608 (2007/10/02)
Twenty-seven sesquiterpenes were isolated from leaves of Cryptomeria japonica.The new compounds included elem-1-en-4,11-diol, 11-acetoxyeudesman-4α-ol, eudesmane-5α,11-diol, 3-eudesmene-1β,11-diol, 1β-acetoxy-3-eudesmen-11-ol, 4-eudesmene-1β,11-diol, 1β-acetoxy-4-eudesmen-11-ol, 7-epi-4-eudesmene-1β,11-diol, 1β-acetoxy-4(15)eudesmen-11-ol.Their structures were determined by chemical and spectral methods. - Key words: Cryptomeria japonica; Taxodiaceae; leaves; sesquiterpenes.
Structures of Eudesmagnolol and Eudeshonokiol, Novel Sesquiterpene-Neolignans Isolated from Magnolia obovata
Fukuyama, Yoshiyasu,Otoshi, Yukio,Nakamura, Kazuhiko,Kodama, Mitsuaki,Sugawara, Michiharu,Nagaswa, Masakazu
, p. 295 - 296 (2007/10/02)
Eudesmagnolol and eudeshonokiol, isolated from the bark of Magnolia obovata, have been assigned to unprecedented structures linked via an ether bond between sesquiterpene, eudesmol, and neolignans, magnolol and honokiol, respectively.
