89000-11-3 Usage
Description
2,4(1H,3H)-Pyrimidinedione, 5-[[(4-methoxyphenyl)thio]methyl]is an organic chemical compound characterized by a molecular formula C13H11N3O3S. It features a pyrimidinedione ring and a 4-methoxyphenylthio group, which is an aromatic thioether. 2,4(1H,3H)-Pyrimidinedione, 5-[[(4-methoxyphenyl)thio]methyl]may have pharmaceutical or industrial applications due to its unique structural features, such as its potential for binding to biological targets or participating in chemical reactions. Further research and analysis of its properties and potential uses could reveal its applications and benefits.
Uses
Used in Pharmaceutical Industry:
2,4(1H,3H)-Pyrimidinedione, 5-[[(4-methoxyphenyl)thio]methyl]is used as a pharmaceutical candidate for its potential binding to biological targets. Its unique structure, including the pyrimidinedione ring and the 4-methoxyphenylthio group, may allow it to interact with specific proteins or enzymes, making it a promising compound for the development of new drugs.
Used in Chemical Reactions:
2,4(1H,3H)-Pyrimidinedione, 5-[[(4-methoxyphenyl)thio]methyl]is used as a reactant in various chemical reactions. Its structural features, such as the pyrimidinedione ring and the aromatic thioether, may enable it to participate in reactions that could lead to the synthesis of new compounds with potential applications in various industries.
Check Digit Verification of cas no
The CAS Registry Mumber 89000-11-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,0,0 and 0 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 89000-11:
(7*8)+(6*9)+(5*0)+(4*0)+(3*0)+(2*1)+(1*1)=113
113 % 10 = 3
So 89000-11-3 is a valid CAS Registry Number.
89000-11-3Relevant articles and documents
Uracil derivatives. IV. Growth-inhibitory activity against L-1210 cells of orotic acid derivatives and synthesis of 1-(β-D-ribofuranosyl)furo[3,4-d]pyrimidine-2,4,7(1H,3H,5H)-trione
Okada,Nakano,Miyake
, p. 3074 - 3083 (1983)
5-(Substituted thiomethyl)-6-carbamoyluracils (IIIb-h) and 5-(substituted thiomethyl)-uracils (Va-h) were prepared and their ability to inhibit the growth of L-1210 cells in vitro was examined. The reaction of silylated furo[3,4-d]pyrimidine-2,4,7(1H,3H,5
