62423-63-6

Upstream product

• 98235-82-6 3,6-dihydro-1-benzyl-5-chloro-2(1H)-pyrimidinone 
• 54326-16-8 5-chloropyrimidin-2-one 
• 100-39-0 benzyl bromide 

Downstream Products

• 103594-71-4 1-benzyl-5-chloro-3,4-dihydro-4-phenylpyrimidin-2(1H)-one 
• 104312-53-0 1-benzyl-5-chloro-3,6-dihydro-6-phenylpyrimidin-2(1H)-one 
• 98235-91-7 (Z)-1-benzyl-5-chloro-4H-4-phenacylidene-2(1H)-pyrimidinone 
• 98235-90-6 1-benzyl-5-chloro-3,4-dihydro-4-phenacyl-2(1H)-pyrimidinone 
• 104312-54-1 1-benzyl-5-chloro-3,4-dihydro-4-methyl-2(1H)-pyrimidinone 
• 115171-61-4 C₂₀H₃₆ClN₂O₄PSi₃ 
• 92-52-4 biphenyl 
• 117170-33-9 1-benzyl-5-chloro-3,6-dihydro-6-ethynylpyrimidin-2(1H)-one 
• 98235-83-7 1-benzyl-5-chloro-3,4-dihydropyrimidin-2(1H)-one 
• 98235-82-6 3,6-dihydro-1-benzyl-5-chloro-2(1H)-pyrimidinone 
• 34790-80-2 1-benzyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone 
• 101946-80-9 1-benzyl-5-chloro-3,4-dihydro-4-phenylethynylpyrimidin-2(1H)-one 
• 101946-73-0 1-benzyl-3,6-dihydro-6-phenylethynyl-2(1H)-pyrimidinone 
• 98235-95-1 3-benzyl-5-chloro-3,4-dihydro-1-methyl-2(1H)-pyrimidinone 

Relevant academic research and scientific papers

Regioselectivity in The Reductive Formation of Dihydro-5-halo-2(1H)-pyrimidinones

5-Chloro-2(1H)-pyrimidinones are reduced by lithium tri-tert-butoxyaluminum hydride to dihydropyrimidinones.Pyrimidines with a substituent capable of conjugation gave the dihydro isomer which has its double bond in conjugation with this substituent.In the

5-Halopyrimid-2-ones

Novel derivatives of pyrimid-2-one having interesting pharmacological properties are described. The compounds of the invention have been found to be of use in the control of, and in particular in the inhibition of the metaphase of malignant tumours and le

1-Benzyl-5-chloro-2-(1H)-pyrimidone

1-Benzyl-5-chloro-2(1H)-pyrimidone possesses pharmacological activity as an antianxiety agent.