4874-13-9 Usage
Uses
Used in Pharmaceutical Industry:
2,4(1H,3H)-Pyrimidinedione, dihydro-1,3-dimethylis utilized as a precursor in the synthesis of various pharmaceutical drugs. Its unique chemical structure allows it to be incorporated into the development of new medications, contributing to the advancement of healthcare and treatment options.
Used in Agricultural Industry:
In the agricultural sector, 2,4(1H,3H)-Pyrimidinedione, dihydro-1,3-dimethylserves as a precursor for the production of agrochemicals. Its incorporation into these compounds can enhance crop protection and contribute to more efficient and sustainable agricultural practices.
Used in Dyes and Pigments Production:
2,4(1H,3H)-Pyrimidinedione, dihydro-1,3-dimethylis also employed in the manufacturing of dyes and pigments. Its chemical properties make it suitable for creating a wide range of colors and hues, which can be used in various applications, such as textiles, plastics, and printing inks.
Used in Therapeutic Research:
Due to its potential biological activities, 2,4(1H,3H)-Pyrimidinedione, dihydro-1,3-dimethylis being studied for its possible therapeutic properties. Researchers are exploring its potential applications in medicine, with the aim of discovering new treatments and therapies that can benefit human health.
Check Digit Verification of cas no
The CAS Registry Mumber 4874-13-9 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,7 and 4 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4874-13:
(6*4)+(5*8)+(4*7)+(3*4)+(2*1)+(1*3)=109
109 % 10 = 9
So 4874-13-9 is a valid CAS Registry Number.
4874-13-9Relevant academic research and scientific papers
Oxidative cleavage of a cyclobutane pyrimidine dimer by photochemically generated nitrate radicals (no(3)*).
Krueger,Wille
, p. 1455 - 1458 (2007/10/03)
[reaction: see text] Photochemically generated nitrate radicals (NO(3)(*)) cleave the stereoisomeric N,N-dimethyl-substituted uracil cyclobutane dimers 1a-d into the monomeric uracil derivative 2 as the major reaction pathway. A preferred splitting of the syn dimers 1a,b was observed. The reaction is expected to proceed through initial one-electron oxidation with formation of an intermediate cyclobutane radical cation 11. In addition to cycloreversion, competing reaction steps of 11, which lead to the observed byproducts, are suggested.
Protonation of the electron adducts of pyrimidine derivatives
Ohkura,Seki
, p. 1024 - 1027 (2007/10/03)
Photolyses of 5-substituted 1,3-dimethyluracils (1a-e: a, R = F; b, R = Cl; c, R = H; d, R = CH3; e, R = p-xylyl) in p-xylene in the presence of trifluoroacetic acid (TFA) afforded 5,6-dihydro-1,3-dimethyl-6-p-methylbenzyluracils (3a-d), 5,6-dihydro-1,3-dimethyl-5-p-methylbenzyluracils (4a-e), and 5,6-dihydro-1,3-dimethyluracils (5a-e) in varying ratios. It is suggested that the 6-isomers (3) are derived from the O(4)-protonated electron adducts of 1, while 4 and 5 are the products from the C(6)-protonated electron adducts. The ratio of (4 + 5) vs. 3 depends on the ionization potentials of the O(4)-protonated intermediates. The formation of 4 + 5 increases with increasing concentration of TFA.
