59456-01-8 Usage
Description
4-Bromo-2-phenylquinazoline, also known as 4-bromo-2-phenyl-1,3-diazanaphthalene, is a heterocyclic compound characterized by its quinazoline core structure. It is a white to light yellow solid that exhibits solubility in organic solvents but is insoluble in water. This chemical compound is recognized for its potential in medicinal chemistry and drug design, serving as a versatile building block for the synthesis of various bioactive molecules. Its applications extend to the development of fluorescence sensors for detecting metal ions in biological and environmental samples, as well as its exploration for anti-cancer and anti-inflammatory properties, positioning it as a significant subject in pharmaceutical research.
Uses
Used in Medicinal Chemistry and Drug Design:
4-Bromo-2-phenylquinazoline is utilized as a building block for the synthesis of bioactive molecules, contributing to the development of new pharmaceutical agents. Its structural properties allow for the creation of diverse compounds with potential therapeutic applications.
Used in Fluorescence Sensing Applications:
In the field of analytical chemistry, 4-Bromo-2-phenylquinazoline is employed as a fluorescence sensor for the detection of metal ions. This capability is particularly valuable for monitoring metal ion concentrations in biological and environmental samples, facilitating research and environmental monitoring efforts.
Used in Pharmaceutical Research:
4-Bromo-2-phenylquinazoline is studied for its potential anti-cancer and anti-inflammatory properties, making it a valuable compound in the search for new treatments and therapies. Its exploration in this area could lead to advancements in medicine, particularly for conditions that are currently challenging to treat.
Used in Chemical Synthesis Industry:
As a key intermediate in the synthesis of various organic compounds, 4-Bromo-2-phenylquinazoline is used in the chemical synthesis industry to produce a range of products, from pharmaceuticals to specialty chemicals, highlighting its importance in the development of new chemical entities.
Check Digit Verification of cas no
The CAS Registry Mumber 59456-01-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,9,4,5 and 6 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 59456-01:
(7*5)+(6*9)+(5*4)+(4*5)+(3*6)+(2*0)+(1*1)=148
148 % 10 = 8
So 59456-01-8 is a valid CAS Registry Number.
59456-01-8Relevant articles and documents
Substituted 2-arylquinazolines as fungicides
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, (2008/06/13)
Fungicidal compositions based on substituted 2-arylquinazolines exhibit antifungal activity particularly against rusts and mildews. The synthesis of new compounds is described and the utility of antifungal compositions is exemplified.
