98629-84-6

Usage

Uses

Used in Pharmaceutical Industry:
TETRAHYDRO-2,4,6-TRIOXO-1(2H)-PYRIMIDINEACETIC ACID ETHYL ESTER is used as a precursor in the synthesis of various drugs, due to its unique molecular structure and versatile chemical properties.
Used in Agricultural Industry:
TETRAHYDRO-2,4,6-TRIOXO-1(2H)-PYRIMIDINEACETIC ACID ETHYL ESTER is used as a precursor in the synthesis of herbicides, due to its unique molecular structure and versatile chemical properties.
Further research and development are essential to explore the full potential and possible applications of TETRAHYDRO-2,4,6-TRIOXO-1(2H)-PYRIMIDINEACETIC ACID ETHYL ESTER in both the pharmaceutical and agricultural industries.

InChI:InChI=1/C8H10N2O5/c1-2-15-7(13)4-10-6(12)3-5(11)9-8(10)14/h2-4H2,1H3,(H,9,11,14)

Upstream product

• 141-82-2 malonic acid 
• 6293-20-5 ethyl hydantoate 

Downstream Products

• 98629-89-1 5,5'-p-nitrophenylmethylenebis<6-methylamino-3-(N-methylcarbamoylmethyl)uracil> 
• 98629-88-0 5,5'-p-chlorophenylmethylenebis<6-methylamino-3-(N-methylcarbamoylmethyl)uracil> 
• 98629-87-9 5,5'-p-fluorophenylmethylenebis<6-methylamino-3-(N-methylcarbamoylmethyl)uracil> 

Relevant academic research and scientific papers

ALKYLATION OF 6-METHOXYURACIL AND A NEW METHOD FOR THE SYNTHESIS OF N-SUBSTITUTED BARBITURIC ACIDS

The alkylation of the metallic salts of 6-methoxyuracil by dimethyl sulfate and alkyl halides leads to the selective formation of 1-alkyl-6-methoxyuracils.The alkylation of these compounds leads to the formation of 1,3-substituted derivatives of 6-methoxyuracil.The acid hydrolysis of 6-methoxyuracils makes it possible to obtain 1- and 1,3-substituted barbituric acids.

Synthesis of Water Soluble 8-Substituted 5-Deazaflavins

By oxidative cyclization of 5,5'-arylmethylenebis(6-methylaminouracil) derivatives with diethyl azodicarboxylate a number of 5-deazaisoalloxazines were synthesized having at the C(8) position a substituent that causes a bathochromic shift varying between 20 and 130 nm, depending on the substituent.To increase the solubility in aqueous media 8-substituted 5-deazaflavins were prepared having a carboxymethyl group at the N(3) position.The carboxymethyl group was introduced prior to the oxidative cyclization.