3333-62-8 Usage
Uses
Used in Pharmaceutical Industry:
7-(2H-naphtho[1,2-d]triazol-2-yl)-3-phenyl-2-benzopyrone is used as a potential anti-cancer agent for its ability to inhibit the activity of enzymes that are often implicated in the progression of cancer. Its unique structure allows it to target and interfere with cellular processes that contribute to tumor growth and metastasis, making it a valuable compound in the search for novel cancer treatments.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 7-(2H-naphtho[1,2-d]triazol-2-yl)-3-phenyl-2-benzopyrone serves as an interesting target for further research and development. Its structure and properties are being investigated to understand its full potential in treating a range of diseases and conditions, with a focus on enhancing its efficacy and reducing potential side effects.
Used in Drug Development:
7-(2H-naphtho[1,2-d]triazol-2-yl)-3-phenyl-2-benzopyrone is utilized in drug development efforts to create new pharmaceuticals that can address unmet medical needs. Its unique chemical structure provides a foundation for the design of innovative drugs that may offer improved therapeutic options for patients suffering from various illnesses.
Check Digit Verification of cas no
The CAS Registry Mumber 3333-62-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,3 and 3 respectively; the second part has 2 digits, 6 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3333-62:
(6*3)+(5*3)+(4*3)+(3*3)+(2*6)+(1*2)=68
68 % 10 = 8
So 3333-62-8 is a valid CAS Registry Number.
InChI:InChI=1/C25H15N3O2/c29-25-21(16-6-2-1-3-7-16)14-18-10-12-19(15-23(18)30-25)28-26-22-13-11-17-8-4-5-9-20(17)24(22)27-28/h1-15H
3333-62-8Relevant academic research and scientific papers
Thermospray Ionization and Tandem Mass Spectrometry of Dyes
Ballard, John M.,Betowski, Leon D.
, p. 575 - 588 (2007/10/02)
Sixteen commercial dye samples and three liquid wastes from organic pigment and dye manufacture have been characterized without prior chromatography by thermospray ionization and low energy collision activated dissociation of protonated molecules using a triple quadrupole mass spectrometer.Many samples contained precursors of the dyes and other by-products of the synthesis.Many of these components were identified by collision-activated dissociation experiments and by inspection of the chemistry of dye manufacture.Detection limits of 20-200 ng in the positive ion mode were obtained for seven dyes of the anthraquinone, triarylmethanem xanthene, coumarin, azo and sulfonated azo dye classes.Under conditions of negative ionization, detection limits for an anthraquinone dye and a sulfonated azo dye were about one order of magnitude higher.
