62423-63-6

Basic information

• Product Name: 2(1H)-Pyrimidinone, 5-chloro-1-(phenylmethyl)-
• CAS NO: 62423-63-6
• Molecular Formula: C11H9ClN2O
• Molecular Weight: 220.658
• Mol File: 62423-63-6.mol
• Article Data: 4

Chemical Properties

• CAS DataBase Reference: 2(1H)-Pyrimidinone, 5-chloro-1-(phenylmethyl)-(CAS DataBase Reference)
• NIST Chemistry Reference: 2(1H)-Pyrimidinone, 5-chloro-1-(phenylmethyl)-(62423-63-6)
• EPA Substance Registry System: 2(1H)-Pyrimidinone, 5-chloro-1-(phenylmethyl)-(62423-63-6)

Safety Data

• Hazardous Substances Data: 62423-63-6(Hazardous Substances Data)

Upstream product

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

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 
• 115171-63-6 1-benzyl-5-chloro-2-oxo-3,4-dihydropyrimidine-4-phosphonic acide 

Relevant articles and documents

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

Selective Alkylation of Ambient 5-Halopyrimidin-2-one Anion

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