81128-01-0 Usage
Uses
Used in Organic Synthesis:
2,4-DIPHENYL-5,6,7,8-TETRAHYDROCHROMENYLIUM TRIFLUOROMETHANESULPHONATE is used as a reagent in organic chemistry reactions for its distinctive structural and reactive properties, facilitating the synthesis of complex organic molecules.
Used in Material Science:
In the field of material science, 2,4-DIPHENYL-5,6,7,8-TETRAHYDROCHROMENYLIUM TRIFLUOROMETHANESULPHONATE is utilized for its potential to contribute to the development of new materials with unique properties, owing to its structural characteristics.
Used in Pharmaceutical Research:
2,4-DIPHENYL-5,6,7,8-TETRAHYDROCHROMENYLIUM TRIFLUOROMETHANESULPHONATE is employed as a research tool in pharmaceutical studies, where its chemical properties are explored for the discovery and development of new drugs.
Used in Drug Development:
In drug development, 2,4-DIPHENYL-5,6,7,8-TETRAHYDROCHROMENYLIUM TRIFLUOROMETHANESULPHONATE is used as a potential candidate in the creation of novel therapeutic agents, capitalizing on its reactivity and structural attributes to address specific medical needs.
Overall, 2,4-DIPHENYL-5,6,7,8-TETRAHYDROCHROMENYLIUM TRIFLUOROMETHANESULPHONATE is a versatile chemical entity with a wide range of applications across different scientific disciplines, making it a valuable asset in the advancement of chemical knowledge and technological innovation.
Check Digit Verification of cas no
The CAS Registry Mumber 81128-01-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,1,2 and 8 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 81128-01:
(7*8)+(6*1)+(5*1)+(4*2)+(3*8)+(2*0)+(1*1)=100
100 % 10 = 0
So 81128-01-0 is a valid CAS Registry Number.
InChI:InChI=1/C21H19O.CHF3O3S/c1-3-9-16(10-4-1)19-15-21(17-11-5-2-6-12-17)22-20-14-8-7-13-18(19)20;2-1(3,4)8(5,6)7/h1-6,9-12,15H,7-8,13-14H2;(H,5,6,7)/q+1;/p-1
81128-01-0Relevant academic research and scientific papers
The Chemistry of Some Bicyclic Pyridinium Anhydrobases
Katritzky, Alan R.,Ueroegdi, Laszlo,Patel, Ranjan C.
, p. 1349 - 1354 (2007/10/02)
The anhydrobase from 5,6,7,8-tetrahydro-2,4-diphenyl-1-p-tolylquinolinium reacts with C-, N-, and S-electrophiles to form adducts and new anhydrobases.The tautomeric structures of the adducts are deduced from spectral evidence.
