100201-53-4 Usage
Uses
Used in Pharmaceutical Synthesis:
2,4(1H,3H)-Pyrimidinedione, 6-(acetyloxy)-5,5-dichlorodihydro-1,3-dimethylis utilized as a key intermediate in the synthesis of pharmaceuticals for its ability to enhance the stability and bioactivity of the resulting compounds. The acetyloxy group serves as a protecting group, facilitating the synthesis process and improving the yield of desired products.
Used in Agrochemical Synthesis:
In the agrochemical industry, 2,4(1H,3H)-Pyrimidinedione, 6-(acetyloxy)-5,5-dichlorodihydro-1,3-dimethylis employed as a building block for the development of new agrochemicals with improved properties. The dichlorodihydro-dimethyl groups contribute to the compound's stability and effectiveness, making it suitable for use in various agricultural applications.
Used in Materials Science:
2,4(1H,3H)-Pyrimidinedione, 6-(acetyloxy)-5,5-dichlorodihydro-1,3-dimethylmay find applications in materials science due to its unique structure and reactivity. Its potential use in the development of new materials with specific properties, such as improved stability or biocompatibility, is currently being explored.
Used in Drug Discovery:
The distinctive structure and reactivity of 2,4(1H,3H)-Pyrimidinedione, 6-(acetyloxy)-5,5-dichlorodihydro-1,3-dimethylmake it a promising candidate for drug discovery. Its potential to serve as a building block for the development of new drugs with novel mechanisms of action and improved therapeutic profiles is being investigated in various research settings.
Check Digit Verification of cas no
The CAS Registry Mumber 100201-53-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,0,2,0 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 100201-53:
(8*1)+(7*0)+(6*0)+(5*2)+(4*0)+(3*1)+(2*5)+(1*3)=34
34 % 10 = 4
So 100201-53-4 is a valid CAS Registry Number.
100201-53-4Relevant academic research and scientific papers
Itahara, Toshio,Ebihara, Reiko,Fujii, Yukiko,Tada, Miki
, p. 1319 - 1322 (1986)
Reaction of thymines with Na2S2O8 in water resulted in selective oxidation of the methyl group at 5-position of thymines.Oxidation of thymines with Na2S2O8 in hydrochloric acid gave 5-chloro-6-hydroxy-5,6-dihydrothymines and in acetic acid containing NaCl gave 6-acetoxy-5-chloro-5,6-dihydrothymines which were converted to 6-alkoxy-5-chloro-5,6-dihydrothymines with alcohols.The reaction of uracils also gave similar products together with 5-chlorouracils.
