38009-11-9 Usage
Chemical Structure
1,3-Dimethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidine-5-carboxamide is a complex compound with a pyrimidine ring structure, two methyl groups, two carbonyl groups, and a carboxamide group.
Family
It belongs to the pyrimidine family of compounds.
Pharmaceuticals
Due to its unique structure, it may have potential applications in the pharmaceutical industry.
Chemical Research
It can be used in chemical research for studying its properties and potential uses.
Building Block
It may serve as a building block for the synthesis of other organic compounds.
Ongoing Research
The exact properties and uses of this compound are still under investigation in the fields of chemistry and pharmaceuticals.
Biological Activity
It may possess biological activity, which could be explored for potential applications in medicine or other areas.
Molecular Weight
The molecular weight of 1,3-Dimethyl-2,4-dioxo-1,2,3,4-tetrahydropyrimidine-5-carboxamide is approximately 170.17 g/mol.
Solubility
The solubility of this compound in various solvents is not explicitly mentioned, but it may vary depending on the solvent's polarity and the compound's functional groups.
Reactivity
The reactivity of this compound with other chemicals or under specific conditions is not detailed, but it may be influenced by the presence of its functional groups, such as the carbonyl and carboxamide groups.
Check Digit Verification of cas no
The CAS Registry Mumber 38009-11-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 3,8,0,0 and 9 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 38009-11:
(7*3)+(6*8)+(5*0)+(4*0)+(3*9)+(2*1)+(1*1)=99
99 % 10 = 9
So 38009-11-9 is a valid CAS Registry Number.
38009-11-9Relevant articles and documents
Chemical models and their mechanistic implications for the transformation of 6-cyanouridine 5′-monophosphate catalyzed by orotidine 5′-monophosphate decarboxylase
Wu, Yuen-Jen,Liao, Chen-Chieh,Jen, Cheng-Hung,Shih, Yu-Chiao,Chien, Tun-Cheng
scheme or table, p. 4821 - 4823 (2010/08/22)
The reactions of 6-cyano-1,3-dimethyluracil have been studied as chemical models to illustrate the mechanism for the transformation of 6-cyanouridine 5′-monophosphate (6-CN-UMP) to barbiturate ribonucleoside 5′-monophosphate (BMP) catalyzed by orotidine 5′-monophosphate decarboxylase (ODCase). The results suggest that the Asp residue in the ODCase active site plays the role of a general base in the transformation.
Pyrimidines. 20. Novel Reactions of 5-Cyano-1,3-dimethyluracil. A Simple Synthesis of Pyridopyrimidines
Su, Tsann-Long,Watanabe, Kyoichi A.
, p. 1261 - 1262 (2007/10/02)
A reaction of 5-cyano-1,3-dimethyluracil (1, R = CN) with acetone in base afforded 1,3,7-trimethylpyridopyrimidine-2,4(1H,3H)-dione (9a) in a moderate yield.From a reaction mixture of 1 (R = CN) with butanone, 1,3,6,7-tetramethyl- and 7-ethyl-1,3-dimethylpyridopyrimidine-2,4(1H,3H)-dione (9b and 9c, respectively) were isolated in low yields.When ethyl cyanoacetate or malononitrile was used in place of the ketone in the above reaction, 7-amino-6-ethoxycarbonyl- and 7-amino-6-cyano-1,3-dimethylpyridopyrimidine-2,4(1H,3H)-dione (14a and 14b, respectively) were obtained in quantitative yields.A plausible mechanism for the formation of bicyclic compounds is discussed.
