13300-13-5 Usage
Uses
Used in Pharmaceutical Synthesis:
2,4(3H,8H)-Pteridinedione, 8-(2-hydroxyethyl)-3-methyl-6,7-diphenylis used as a key building block in the synthesis of various pharmaceuticals for its versatile reactivity and functional groups, contributing to the development of new drugs with improved therapeutic properties.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, 2,4(3H,8H)-Pteridinedione, 8-(2-hydroxyethyl)-3-methyl-6,7-diphenylis utilized for its potential biological activities, such as its antitumor and antioxidant properties, making it a promising candidate for the discovery and development of novel therapeutic agents.
Used in Organic Compounds Synthesis:
This pteridinedione compound is also used as a building block in the synthesis of various organic compounds, leveraging its unique structure and reactivity to create new molecules with specific applications in different industries.
Check Digit Verification of cas no
The CAS Registry Mumber 13300-13-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,3,0 and 0 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 13300-13:
(7*1)+(6*3)+(5*3)+(4*0)+(3*0)+(2*1)+(1*3)=45
45 % 10 = 5
So 13300-13-5 is a valid CAS Registry Number.
13300-13-5Relevant academic research and scientific papers
Pteridines, LXXI. - Synthesis and Photochemical Behaviour of 8- Substituted Lumazines
Ram, Vishnu J.,Knappe, Wolfgang R.,Pfleiderer, Wolfgang
, p. 762 - 779 (2007/10/02)
The 8-substituted lumazines 34-69 have been synthesized from 6-chloro-5-nitrouracil (1) and its 3-methyl derivative 2 via the corresponding 6-amino-5-nitrouracils 3-26, substituted at the amino nitrogen.The photochemical properties of the 8-substituted lumazines have been investigated.Various photoreactions were observed depending on the chemical nature of the N-8-side-chain and leading to an easy photodealkylation of the β-hydroxy-, β-methoxy-, and β-aminoethyl derivatives 34-44.Increasing donor properties of the β-substituent enhances the photolability which is expressed in a Norrish-type II cleavage reaction to the corresponding lumazines 70-75. 8-Cycloalkyllumazines 52-54 show photoreduction to 7,8-dihydrolumazines 76-78.The newly synthesized 8-substituted lumazine derivatives have been characterized by elementary analyses and UV spectra.Structural peculiarities due to the various substituents in position 6, 7, and 8 will be discussed.
