Weight | 110.116 g/mol |
---|---|
Formula | C5H6N2O |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 1 |
5-Methoxypyrimidine (31458-33-0)
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- Photochemistry of aromatic compounds : Mechanism of the amine-accelerated photodebromination of 5-bromo-2-methoxypyrimidine (Tetrahedron, 1972)
- The synthesis of some 5-methoxypyrimidine nucleosides (Journal of Heterocyclic Chemistry, 1972)
- Long-acting sulphonamides. III. New synthesis of 2-sulphanilamido-5-methoxypyrimidine (Collection of Czechoslovak Chemical Communications, 1964)
- A facile one-pot preparation of 2-methyl-and 2-phenyl-4- fluoro-5-trifluoromethyl-6-methoxypyrimidine from methyl 2-hydryl-2-(F-methyl)-F-propyl ether (Journal of Fluorine Chemistry, 1985)
- Syntheses and Transformations of 4-Amino-2-methylthio- and 4-Amino-2-methoxypyrimidine-5-carboxamide Oximes (Heterocycles, 1985)
- [Clinical studies with 2-sulfanilamido-5-methoxypyrimidine]. (Drug Research, 1961)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCOC1=CN=CN=C1
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InChIKeyJIADELSANNMYFC-UHFFFAOYSA-N
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Synthesis
Reactant
+
Methyl hydroperoxide
(Dakin oxidation)
Similar Compounds
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pyrimidin-4-ol
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(274-95-3)
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(62802-38-4)
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(111336-11-9)
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Tebupirimfos
(96182-53-5)
1 alternate name
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2-methoxypyrimidin-4-amine
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4-Chloro-6-methoxypyrimidine
(26452-81-3)
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2-methylpyrimidine-5-carbaldehyde
(90905-33-2)
1 alternate name
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2-Methoxy-5-nitropyrimidine
(14001-69-5)
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2-Bromo-3-methoxypyridine
(24100-18-3)
1 alternate name
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