486-90-8 Usage
Uses
Used in Solar Energy Systems:
Thermospine is utilized as a thermal energy storage medium for capturing and releasing heat generated by solar panels. Its phase change properties allow for the efficient storage of solar energy during the day and its release during periods of demand, enhancing the overall performance and sustainability of solar energy systems.
Used in Building Insulation:
In the construction industry, thermospine serves as a heat management component in building insulation. Its ability to store and release heat at specific temperatures contributes to maintaining a stable indoor climate, reducing the need for additional heating or cooling, and improving energy efficiency in buildings.
Used in Industrial Heat Storage:
Thermospine is employed as a heat storage solution in various industrial processes. Its capacity to absorb and release large amounts of heat at precise temperatures ensures optimal thermal management, enhancing process efficiency and reducing energy waste in industrial applications.
Check Digit Verification of cas no
The CAS Registry Mumber 486-90-8 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 4,8 and 6 respectively; the second part has 2 digits, 9 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 486-90:
(5*4)+(4*8)+(3*6)+(2*9)+(1*0)=88
88 % 10 = 8
So 486-90-8 is a valid CAS Registry Number.
InChI:InChI=1/C15H20N2O/c18-15-6-3-5-14-11-8-12(10-17(14)15)13-4-1-2-7-16(13)9-11/h3,5-6,11-13H,1-2,4,7-10H2/t11-,12+,13-/m0/s1
486-90-8Relevant academic research and scientific papers
The Enantioselective Total Synthesis of Bisquinolizidine Alkaloids: A Modular “Inside-Out” Approach
Scharnagel, Dagmar,Goller, Jessica,Deibl, Nicklas,Milius, Wolfgang,Breuning, Matthias
, p. 2432 - 2435 (2018/02/16)
Bisquinolizidine alkaloids are characterized by a chiral bispidine core (3,7-diazabicyclo[3.3.1]nonane) to which combinations of an α,N-fused 2-pyridone, an endo- or exo-α,N-annulated piperidin(on)e, and an exo-allyl substituent are attached. We developed a modular “inside-out” approach that permits access to most members of this class. Its applicability was proven in the asymmetric synthesis of 21 natural bisquinolizidine alkaloids, among them more than ten first enantioselective total syntheses. Key steps are the first successful preparation of both enantiomers of C2-symmetric 2,6-dioxobispidine by desymmetrization of a 2,4,6,8-tetraoxo precursor, the construction of the α,N-fused 2-pyridone by using an enamine-bromoacrylic acid strategy, and the installation of endo- or, optionally, exo-annulated piperidin(on)es.
A flexible strategy for the synthesis of tri- and tetracyclic lupin alkaloids: Synthesis of (+)-cytisine, (±)-anagyrine, and (±)-thermopsine
Gray, Diane,Gallagher, Timothy
, p. 2419 - 2423 (2007/10/03)
(Chemical Equation Presented) Looping the lupin: A general synthetic strategy for the construction of the lupin alkaloids has been defined and involves sequential formation of the N1-C10 and C6-C7 bonds, which are common to compounds of this class of natu
