76457-03-9 Usage
Uses
Used in Organic Chemistry:
1-(3,3,5-triphenyl-3H-pyrrol-2-yl)phthalazine is used as a building block for the synthesis of other complex organic molecules, taking advantage of its diverse and reactive structural components.
Used in Medicinal Chemistry:
In the field of medicinal chemistry, 1-(3,3,5-triphenyl-3H-pyrrol-2-yl)phthalazine is used as a potential candidate for the development of new drugs, due to its potential biological activities such as antibacterial, antifungal, or antiviral properties.
Used in Material Science:
1-(3,3,5-triphenyl-3H-pyrrol-2-yl)phthalazine's conjugated aromatic system makes 1-(3,3,5-triphenyl-3H-pyrrol-2-yl)phthalazine a candidate for use in material science, where its electronic and optical properties could be harnessed for various applications.
Check Digit Verification of cas no
The CAS Registry Mumber 76457-03-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,6,4,5 and 7 respectively; the second part has 2 digits, 0 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 76457-03:
(7*7)+(6*6)+(5*4)+(4*5)+(3*7)+(2*0)+(1*3)=149
149 % 10 = 9
So 76457-03-9 is a valid CAS Registry Number.
76457-03-9Relevant academic research and scientific papers
Riessert Compound Studies.XXXV. Acid-Catalyzed Condensations of the Phtalazine Reissert Compound and Condensations of Phthalazine Reissert Compound Salt
Bhattacharjee, D.,Popp, F. D.
, p. 1035 - 1040 (2007/10/02)
The phtalazine Reissert compound hydrofluoroborate undergoes condensation with alkynes to give pyrrolophthalazines and with alkenes to give 2(1-phthalazyl)pyrroles.The phthalazine Reissert compound undergoes acid catalyzed condensations with some alkenes but the intermediate is of sufficient stability to be isolated.This type of intermediate can also be isolated in the acid-catalyzed hydrolysis of the phthalazine Reissert compound.
