166990-10-9 Usage
Uses
Used in Pharmaceutical Applications:
[2]Benzopyrano[4,3-a]carbazol-2-ol,1,2,3,4,4a,5,13,13c-octahydro-2,5,5,7-tetramethyl-, (2R,4aS,13cS)-rel-(-)-(9CI) is used as a pharmaceutical agent for its potential therapeutic properties. [2]Benzopyrano[4,3-a]carbazol-2-ol,1,2,3,4,4a,5,13,13c-octahydro-2,5,5,7-tetramethyl-, (2R,4aS,13cS)-rel-(-)-(9CI)'s unique structure may allow it to interact with biological targets in ways that could lead to the development of new drugs or treatments for various diseases.
Used in Materials Science:
In the field of materials science, [2]Benzopyrano[4,3-a]carbazol-2-ol,1,2,3,4,4a,5,13,13c-octahydro-2,5,5,7-tetramethyl-, (2R,4aS,13cS)-rel-(-)-(9CI) may be utilized for the development of novel materials with specific properties. Its structural features could contribute to the creation of materials with tailored characteristics for use in various applications, such as sensors, catalysts, or advanced materials with unique mechanical or electronic properties.
Used in Organic Chemistry Research:
[2]Benzopyrano[4,3-a]carbazol-2-ol,1,2,3,4,4a,5,13,13c-octahydro-2,5,5,7-tetramethyl-, (2R,4aS,13cS)-rel-(-)-(9CI) serves as a subject of study in organic chemistry research. Its synthesis and properties can provide insights into the behavior of complex organic molecules and contribute to the understanding of stereochemistry and molecular interactions. This knowledge can further the development of new synthetic methods and the discovery of new compounds with potential applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 166990-10-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,6,6,9,9 and 0 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 166990-10:
(8*1)+(7*6)+(6*6)+(5*9)+(4*9)+(3*0)+(2*1)+(1*0)=169
169 % 10 = 9
So 166990-10-9 is a valid CAS Registry Number.
166990-10-9Relevant academic research and scientific papers
Dethe, Dattatraya H.,Das, Saikat,Dherange, Balu D.,Mahapatra, Samarpita
, p. 8347 - 8350 (2015)
First enantiospecific total syntheses of the cannabinol-skeletal carbazole alkaloids murrayamines-O and -P isolated from root barks of Murraya euchrestifoli, have been accomplished by highly diastereoselective, Lewis acid catalyzed coupling reactions of commercially available monoterpenes with carbazole derivative, which in addition to confirming the structure also established the absolute configuration of the natural products. Synthesis of both natural products and their enantiomers was achieved with high atom economy, in a protecting-group free manner and in six steps longest linear sequence from commercially available aniline derivative and verbenol.
