20489-45-6 Usage
Uses
Used in Pharmaceutical Industry:
(2R)-1,2,3,4,6,7,8,8a-Octahydro-α,α,8β,8aβ-tetramethyl-2-naphthalenemethanol is used as an intermediate in the synthesis of various pharmaceutical compounds. Its unique structure allows for the development of new drugs with potential therapeutic applications.
Used in Chemical Industry:
In the chemical industry, (2R)-1,2,3,4,6,7,8,8a-Octahydro-α,α,8β,8aβ-tetramethyl-2-naphthalenemethanol can be used as a building block for the creation of more complex molecules. Its versatile structure makes it a valuable component in the synthesis of various specialty chemicals.
Used in Flavor and Fragrance Industry:
(2R)-1,2,3,4,6,7,8,8a-Octahydro-α,α,8β,8aβ-tetramethyl-2-naphthalenemethanol may also find applications in the flavor and fragrance industry due to its potential aromatic properties. It could be used to create unique scents or enhance the flavor profiles of various products.
Used in Research and Development:
Due to its unique structure and properties, (2R)-1,2,3,4,6,7,8,8a-Octahydro-α,α,8β,8aβ-tetramethyl-2-naphthalenemethanol can be a valuable compound for research and development purposes. It may be used in the study of organic chemistry, molecular biology, and other related fields to explore new reactions and applications.
Check Digit Verification of cas no
The CAS Registry Mumber 20489-45-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,0,4,8 and 9 respectively; the second part has 2 digits, 4 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 20489-45:
(7*2)+(6*0)+(5*4)+(4*8)+(3*9)+(2*4)+(1*5)=106
106 % 10 = 6
So 20489-45-6 is a valid CAS Registry Number.
InChI:InChI=1/C15H26O/c1-11-6-5-7-12-8-9-13(14(2,3)16)10-15(11,12)4/h7,11,13,16H,5-6,8-10H2,1-4H3/t11-,13-,15+/m1/s1
20489-45-6Relevant academic research and scientific papers
Naef, Ferdinand,Decorzant, Rene,Thommen, Walter
, p. 2212 - 2223 (1982)
A stereocontrolled route to racemic eremophilane and valencane sesquiterpenes is described via a common inetrmediate 15, accessible from an intramolecular Diels-Alder rection. 13C-NMR-shift assignments of the bicyclic intermediates and products are presented.
The Preparation and Microbiological Hydroxylation of 10β,11-Oxido-4α,5α,7β-eremophilane
Arantes, Simone F.,Hanson, James R.,Hitchcock, Peter B.
, p. 1415 - 1438 (2007/10/03)
The preparation of 10β,11-oxido-4α,5α,7β-eremophilane by the oxymercuration of valencene, its microbiological hydroxylation at C-1, C-3, C-6, C-7 and C-8 by the fungus, Mucor plumbeus, and the X-ray crystal structures of two of the metabolites, are described.
