93787-99-6 Usage
Uses
Used in Pharmaceutical Industry:
6-ethoxy-1,3-dimethyl-pyrimidine-2,4-dione is used as a chemical intermediate in the synthesis of various pharmaceuticals. Its unique structure and properties make it a valuable component in the development of new drugs with potential therapeutic applications.
Used in Agrochemical Industry:
In the agrochemical industry, 6-ethoxy-1,3-dimethyl-pyrimidine-2,4-dione serves as an intermediate in the production of agrochemicals, contributing to the development of effective pesticides and other agricultural chemicals.
Used in Research and Development:
6-ethoxy-1,3-dimethyl-pyrimidine-2,4-dione is utilized in research and development for its potential anticonvulsant and antihypertensive properties. Scientists and researchers explore its therapeutic potential in treating various medical conditions, such as epilepsy and hypertension.
Used in Drug Delivery Systems:
Although not explicitly mentioned in the provided materials, 6-ethoxy-1,3-dimethyl-pyrimidine-2,4-dione could potentially be used in drug delivery systems to improve the bioavailability and efficacy of pharmaceuticals. Its unique chemical properties may allow for the development of novel drug delivery methods, enhancing the therapeutic outcomes of various treatments.
It is important to reiterate that due to the potential health hazards associated with 6-ethoxy-1,3-dimethyl-pyrimidine-2,4-dione, it should be handled and used with caution, adhering to proper safety protocols and guidelines.
Check Digit Verification of cas no
The CAS Registry Mumber 93787-99-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,3,7,8 and 7 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 93787-99:
(7*9)+(6*3)+(5*7)+(4*8)+(3*7)+(2*9)+(1*9)=196
196 % 10 = 6
So 93787-99-6 is a valid CAS Registry Number.
InChI:InChI=1/C8H12N2O3/c1-4-13-7-5-6(11)9(2)8(12)10(7)3/h5H,4H2,1-3H3
93787-99-6Relevant academic research and scientific papers
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.
ALKYLATION OF 1,3-DIMETHYLBARBITURIC ACID BY ALKYL IODIDES
Krasnov, K. A.,Slesarev, V. I.,Artem'eva, Z. L.
, p. 1402 - 1405 (2007/10/02)
The alkylation of 1,3-dimethylbarbituric acid by methyl iodide, ethyl iodide, and isopropyl iodide in the presence of triethylamine was investigated.The kinetics of the process were studied, and it was shown that the steric and electronic factors affect the rate of the alkylation reactions.Only the products from alkylation at the C5 atom are formed in the case of methyl iodide, and concurrent alkylation at the C5 and O4(6) atoms is observed with ethyl iodide and isopropyl iodide.
