83217-77-0

Basic information

• Product Name: 2-(4-CHLOROPHENYL)-6-HYDROXY-4(3H)-PYRIMIDINONE
• Synonyms: 2-(4-CHLOROPHENYL)-6-HYDROXY-4(3H)-PYRIMIDINONE
• CAS NO: 83217-77-0
• Molecular Formula: C₁₀H₇ClN₂O₂
• Molecular Weight: 0
• Mol File: 83217-77-0.mol
• Article Data: 3

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-(4-CHLOROPHENYL)-6-HYDROXY-4(3H)-PYRIMIDINONE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-(4-CHLOROPHENYL)-6-HYDROXY-4(3H)-PYRIMIDINONE(83217-77-0)
• EPA Substance Registry System: 2-(4-CHLOROPHENYL)-6-HYDROXY-4(3H)-PYRIMIDINONE(83217-77-0)

Safety Data

• Hazardous Substances Data: 83217-77-0(Hazardous Substances Data)

Upstream product

• 19068-82-7 2-(4-chloro-phenyl)-4,6-diethoxy-pyrimidine 
• 14401-51-5 4-chlorobenzamidine hydrochloride 
• 6487-93-0 4-chlorophenylacetamidine hydrochloride 
• 105-53-3 diethyl malonate 
• 19563-04-3 p-chlorobenzamidine 

Downstream Products

• 1394124-10-7 methyl 2-(2-(6-chloro-2-(4-chlorophenyl)pyrimidin-4-yloxy)phenyl)-3,3-dimethoxypropanoate 
• 1394124-11-8 (E)-methyl 2-(2-(6-chloro-2-(4-chlorophenyl)pyrimidin-4-yloxy)phenyl)-3-(methoxy)acrylate 
• 1394124-19-6 (E)-methyl 2-(2-(2-(4-chlorophenyl)-6-(2-cyanophenoxy)pyrimidin-4-yloxy)phenyl)-3-(methoxy)acrylate 
• 26870-72-4 4,6-dichloro-2-(4-chlorophenyl)-pyrimidine 

Relevant articles and documents

Synthesis and antifungal activities of new type β-methoxyacrylate- based strobilurin analogues

Strobilurins have become one of the most important classes of agricultural fungicides. To discover new strobilurin derivatives with high activity against resistant pathogens, a series of novel β-methoxyacrylate analogues were designed and synthesized by integrating substituted pyrimidine with a strobilurin pharmacophore. The compounds were confirmed and characterized by infrared, 1H nuclear magnetic resonance, elemental analysis and mass spectroscopy. The bioassays indicated that most of the compounds 1 exhibited potent antifungal activity against Colletotrichum orbiculare, Botrytis cinerea Pers and Phytophthora capsici Leonian at the concentration of 50 μg/mL. Exhilaratingly, compound 1a (R=methyl) showed better antifungal activity against all the tested fungi than the commercial strobilurin fungicide azoxystrobin. Copyright

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