7392-82-7 Usage
Uses
Used in Pharmaceutical Industry:
2,4(1H,3H)-Pyrimidinedione, dihydro-6-hydroxy-1,3-dimethylis used as a synthetic intermediate for the production of various pharmaceuticals. Its unique chemical structure allows it to be incorporated into the synthesis of a wide range of drug molecules, contributing to the development of new therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical industry, 2,4(1H,3H)-Pyrimidinedione, dihydro-6-hydroxy-1,3-dimethylis utilized as a synthetic intermediate for the development of agrochemicals, such as pesticides and herbicides. Its incorporation into these products can enhance their effectiveness in controlling pests and weeds, thereby improving crop yields and quality.
Used in Organic Synthesis:
As a building block in organic synthesis, 2,4(1H,3H)-Pyrimidinedione, dihydro-6-hydroxy-1,3-dimethylis employed in the synthesis of various organic compounds. Its versatile chemical properties enable it to be used in the preparation of a wide array of molecules, including those with potential applications in materials science, pharmaceuticals, and agrochemicals.
Used in Research and Development:
2,4(1H,3H)-Pyrimidinedione, dihydro-6-hydroxy-1,3-dimethylis also used in research and development settings to explore its potential biological and pharmacological activities. Further studies are needed to fully understand its properties and to identify new applications for 2,4(1H,3H)-Pyrimidinedione, dihydro-6-hydroxy-1,3-dimethyl- in various fields, such as medicine, agriculture, and materials science.
Check Digit Verification of cas no
The CAS Registry Mumber 7392-82-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,9 and 2 respectively; the second part has 2 digits, 8 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 7392-82:
(6*7)+(5*3)+(4*9)+(3*2)+(2*8)+(1*2)=117
117 % 10 = 7
So 7392-82-7 is a valid CAS Registry Number.
7392-82-7Relevant academic research and scientific papers
γ-Radiolysis of 1,3-Dimethyluracil in N2O-Saturated Aqueous Solutions
Al-Sheikhly, Mohamed,Sonntag, Clemens von
, p. 1622 - 1629 (2007/10/02)
The γ-radiolysis of N2O-saturated aqueous solutions generates OH radicals and a small amount of H atoms.In 1,3-dimethyluracil solutions (10-3 M) these radicals add mainly to the 5-position of the C(5)-C(6) double bond of the solute.The resulting products have been identified by GC-MS after trimethylsilylation.The major products (G values in brackets) are dimers of the C(5)-OH-adduct radicals (3.4), 5,6-dihydro-5,6-dihydroxy-1,3-dimethyluracil (0.85), 5,6-dihydro-5-hydroxy-1,3-dimethyluracil (0.75), dimer of the C(5)-OH-adduct with the C(5)-H-adduct radical (0.2) and 5,6-dihydro-6-hydroxy-1,3-dimethyluracil (0.2).G(1,3-dimethyluracil consumption) has been found to be 5.7.The major reaction in this system is the dimerisation of the primary radicals.To a small extent the primary radicals also disproportionate by electron transfer to give the glycol 5,6-dihydro-5,6-dihydroxy-1,3-dimethyluracil as one of the products.Radiolytically formed H2O2 which could oxidise the C(5)-OH-adduct radical does not contribute to the formation of the glycol because the H2O2 yield is not reduced with respect to its expected "molecular yield" (G = 0.75).In contrast to the uracil system where it has been reported that drastic changes in radiolytic yields occur on going from neutral to alkaline irradiation conditions no such changes have been observed with 1,3-dimethyluracil.However, an acid-catalysed rearrangement from the C(5)-OH-adduct to the C(6)-OH-adduct radical is observed in the present system. - Keywords: Hydroxyl Radicals, Electron Transfer Reactions, Radical Reactions, DNA Model Systems
