1297613-73-0 Usage
Uses
Used in Pharmaceutical Applications:
(11aR)-10,11,12,13-Tetrahydro-5-hydroxy-3,7-di-1-naphthalenyl-diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin-5-oxide is used as a pharmaceutical agent for its potential therapeutic properties. Its unique structure may offer novel mechanisms of action in treating various diseases, and further research is required to explore its full potential in this field.
Used in Materials Science:
In the field of materials science, (11aR)-10,11,12,13-Tetrahydro-5-hydroxy-3,7-di-1-naphthalenyl-diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin-5-oxide is used as a component in the development of new materials with specific properties. Its chemical structure may contribute to the creation of advanced materials with applications in various industries.
Used in Chemical Research:
(11aR)-10,11,12,13-Tetrahydro-5-hydroxy-3,7-di-1-naphthalenyl-diindeno[7,1-de:1',7'-fg][1,3,2]dioxaphosphocin-5-oxide serves as a subject of interest in chemical research for its unique structure and potential reactivity. It may be used to study new chemical reactions, mechanisms, and the development of novel synthetic pathways.
Check Digit Verification of cas no
The CAS Registry Mumber 1297613-73-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,9,7,6,1 and 3 respectively; the second part has 2 digits, 7 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 1297613-73:
(9*1)+(8*2)+(7*9)+(6*7)+(5*6)+(4*1)+(3*3)+(2*7)+(1*3)=190
190 % 10 = 0
So 1297613-73-0 is a valid CAS Registry Number.
1297613-73-0Relevant academic research and scientific papers
SPINOL-derived phosphoric acids: Synthesis and application in enantioselective Friedel-Crafts reaction of indoles with imines
Xu, Fangxi,Huang, Dan,Han, Chao,Shen, Wei,Lin, Xufeng,Wang, Yanguang
, p. 8677 - 8680 (2011/02/26)
A new class of chiral phosphoric acids with spirobiindane as scaffold were conveniently synthesized from (S)-1,1′-spirobiindane-7,7′-diol ((S)-SPINOL) and employed to catalyze the asymmetric Friedel-Crafts reaction of indoles with imines to afford 3-indol
