CAS 1194-22-5: 6-Hydroxy-2-methyl-4(1H)-pyrimidinone
Formula:C5H6N2O2
InChI:InChI=1S/C5H6N2O2/c1-3-6-4(8)2-5(9)7-3/h2H,1H3,(H2,6,7,8,9)
InChI key:InChIKey=BPSGVKFIQZZFNH-UHFFFAOYSA-N
SMILES:O=C1C=C(O)N=C(C)N1
Synonyms:- 2-Methyl-4,6-Dihydroxy Pyrimidine
- 2-Methyl-4,6-dihydroxypyrimidine
- 2-Methyl-4,6-hydroxypyrimidine
- 2-Methyl-4,6-pyrimidinediol
- 2-Methyl-Pyrimidine-4,6-Diol
- 4(1H)-Pyrimidinone, 6-hydroxy-2-methyl-
- 4,6-Dihydroxy-2-methylpyrimidine
- 4,6-Dihydroxyl-2-Methylpyrimidine
- 4,6-Pyrimidinediol, 2-methyl-
- 4,6-Pyrimidinediol,2-methyl- (6CI,7CI)
- 6-Hydroxy-2-methyl-4(1H)-pyrimidinone
- See more synonyms
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Found 4 products.
6-hydroxy-2-methyl-3,4-dihydropyrimidin-4-one
CAS:6-hydroxy-2-methyl-3,4-dihydropyrimidin-4-onePurity:97+%Molecular weight:126.11g/mol4(1H)-Pyrimidinone, 6-hydroxy-2-methyl-
CAS:Formula:C5H6N2O2Purity:97%Color and Shape:SolidMolecular weight:126.11334,6-Dihydroxy-2-methylpyrimidine
CAS:4,6-Dihydroxy-2-methylpyrimidine is an organic compound that is synthesized by the reaction of 2-chloroethanol with ethyl chloroformate and nitroethane in the presence of a magnesium salt. The synthesis can be done systematically or by chance. 4,6-Dihydroxy-2-methylpyrimidine can be formed by the hydrolysis of ethyl esters with a metallacycle. Its acidic properties are due to its electron withdrawing groups. The systematic synthesis is carried out in two steps: 1) formation of the monomers from ethyl chloroformate and nitroethane; 2) condensation of the monomers to form 4,6-dihydroxy-2-methylpyrimidine. This synthesis requires hydroxide solution and chloroformate as well as a base such as sodium hydroxide or potassium hydroxide. The chemical reaction mechanism is basedFormula:C5H6N2O2Purity:Min. 95%Molecular weight:126.11 g/mol2-Methyl-4,6-dihydroxypyrimidine
CAS:Purity:97.0%Color and Shape:Solid, Brown powderMolecular weight:126.11499786376953
