35218-98-5

Upstream product

• 81077-95-4 5-bromo-1,3-dimethyl-6-phenylthiouracil 
• 6972-27-6 1,3-Dimethyl-6-chlorouracil 
• 930-69-8 sodium thiophenolate 
• 127-19-5 N,N-dimethyl acetamide 

Downstream Products

• 81077-95-4 5-bromo-1,3-dimethyl-6-phenylthiouracil 
• 135581-67-8 1-(1,3-Dimethyl-2,4-dioxo-6-phenylsulfanyl-1,2,3,4-tetrahydro-pyrimidin-5-ylmethyl)-pyridinium; chloride 
• 135581-68-9 1,3,5-Trimethyl-6-(4-nitro-benzylsulfanyl)-1H-pyrimidine-2,4-dione 

Relevant academic research and scientific papers

Synthesis of substituted uracils by the reactions of halouracils with selenium, sulfur, oxygen and nitrogen nucleophiles under focused microwave irradiation

Under microwave irradiation, the nucleophilic substitution reactions of halouracils with selenium, sulfur, oxygen and nitrogen nucleophiles was complete within several minutes with yields up to 99%. The method using microwave irradiation is superior to th

Reductive Debromination and Coupling Reaction in the Thermolysis of 5-Bromouracils in N,N-Dialkylamides. Cleavage of the C(5)-Bromine bond by an Initial Electron-transfer Process

Thermolysis of various 5-bromouracils (1) in N,N-dialkylamides results in the formation of methylenebisuracils (2) and reductive debrominated products (3) via cleavage of the C(5)-Br bond; the latter involves a one-electron transfer process.The product distribution between (2) and (3) depends upon the nature of substituents in the uracil ring.