130634-04-7

Usage

Uses

Used in Pharmaceutical Industry:
2,4(1H,3H)-Pyrimidinedione, 1,3-dimethyl-6-[[2-[[(4-methylphenyl)sulfonyl]oxy]ethyl]amino]may be used as a pharmaceutical or biologically active compound for various applications. Its specific uses and properties would need to be determined through further research and testing.

Upstream product

• 5770-44-5 6-(2-hydroxyethylamino)-1,3-dimethylpyrimidine-2,4(1H,3H)-dion 
• 98-59-9 p-toluenesulfonyl chloride 
• 6972-27-6 1,3-Dimethyl-6-chlorouracil 
• 141-43-5 ethanolamine 
• 584-08-7 potassium carbonate 
• 6642-31-5 6-Amino-1,3-dimethylbarbituric acid 

Downstream Products

• 130634-66-1 1,3-dimethyl-6-{2-[4-(4-nitrophenyl)piperazin-1yl]ethylamino}-2,4(1H,3H)-pyrimidinedione 
• 130636-43-0 1,3-dimethyl-6-[2-(N-[2-hydroxyethyl]-3-[4-nitrophenyl]propylamino)ethylamino]-2,4(1H,3H)-pyrimidinedione 
• 130656-51-8 Shinbit 
• 130636-42-9 6-(2-{Ethyl-[3-(4-nitro-phenyl)-propyl]-amino}-ethylamino)-1,3-dimethyl-1H-pyrimidine-2,4-dione 

Relevant academic research and scientific papers

A method for preparing high-purity hydrochloric acid Nepal non-Kalland

The invention discloses a preparation method of nifekalant hydrochloride. The preparation method comprises the following steps of: performing aminolysis on 6-imino-1,3-dimethyluracil to obtain 1,3-dimethyl-6-(2-ethoxy)aminouracil; esterfying 1,3-dimethyl-

Pyrimidinedione derivative compounds, method for preparing same, and antiarrythmic agents containing same

A pyrimidinedione derivative compound has a basic backbone in which a 4-oxobenzopyran ring group part and a pyrimidinedione part are linked by a structure comprising an alkyl chain containing at least two nitrogen atoms and one oxygen. The pyrimidinedione

Synthesis and pharmacological studies of N-substituted 6-[(2- aminoethyl)amino]-1,3-dimethyl-2,4(1H,3H)-pyrimidinediones, novel class III antiarrhythmic agents

A series of 6-[(2-aminoethyl)amino]-1,3-dimethyl-2,4(1H,3H)- pyrimidinedione derivatives were synthesized and studied for their class III electrophysiological activity and class II (β-blocking) effects in in vitro and in vivo models. Structure-activity re

Pyrimidinedione compounds, method of producing the same and antiarrythmic agents containing the same

A pyrimidinedione derivative compound has a basic backbone in which a phenyl group part and a pyrimidinedione part are linked by a structure comprising an alkyl chain containing at least two nitrogen atoms. The pyrimidinedione derivative is useful for a medical treatment of cardiac arrhythmias.