13300-12-4 Usage
Uses
Used in Pharmaceutical Industry:
2,4(3H,8H)-Pteridinedione, 8-(2-hydroxyethyl)-6,7-diphenylis used as a precursor in the synthesis of pharmaceutical drugs for its potential therapeutic benefits. The hydroxyethyl group and the pteridine core structure contribute to its utility in developing new drugs with enhanced biological activity.
Used in Chemical Research:
In the field of chemical research, 2,4(3H,8H)-Pteridinedione, 8-(2-hydroxyethyl)-6,7-diphenylserves as an intermediate for the synthesis of various biologically active compounds. Its unique structure allows for further functionalization and exploration of its properties in different chemical reactions.
Used in Industrial Applications:
2,4(3H,8H)-Pteridinedione, 8-(2-hydroxyethyl)-6,7-diphenylis also utilized in various industrial applications due to its potential as a building block for the development of new materials and compounds with specific properties. Its versatility in chemical synthesis makes it a valuable component in the creation of innovative products.
Check Digit Verification of cas no
The CAS Registry Mumber 13300-12-4 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 2 respectively.
Calculate Digit Verification of CAS Registry Number 13300-12:
(7*1)+(6*3)+(5*3)+(4*0)+(3*0)+(2*1)+(1*2)=44
44 % 10 = 4
So 13300-12-4 is a valid CAS Registry Number.
13300-12-4Relevant 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.
