Weight | 125.131 g/mol |
---|---|
Formula | C5H7N3O |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 2 |
Aromatic Rings | 1 |
Rotatable Bonds | 0 |
2-Amino-4-hydroxy-6-methylpyrimidine (3977-29-5)
2-amino-6-methylpyrimidin-4-one
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- Environmental photodegradation of pyrimidine fungicides Kinetics of the visible-light- promoted interactions between riboflavin and 2- amino-4-hydroxy-6-methylpyrimidine (Canadian Journal of Chemistry, 2002)
- The hydrazinolysis of heterocyclic compounds. II. 6-Amino-4-hydroxy-1-methylpyrimidine-2(1H)-thione and related compounds (Australian Journal of Chemistry, 1975)
- Kinetics of the dye sensitized photooxidation of 2-amino-4-hydroxy-6-methylpyrimidine, a model compound for some fungicides (Journal of Photochemistry and Photobiology A-chemistry, 2000)
- Macrolide ring closure. Silver ion promoted lactonization of -hydroxy thiolesters of 2-amino-4-mercapto-6-methylpyrimidine (Tetrahedron Letters, 1978)
- Synthesis, characterization and supramolecular structure of three new Cu(II) and Ni(II) complexes with the potentially bidentate ligand 2-amino-6-methylpyrimidin-4(1H)-one (AMPO) (Inorganica Chimica Acta, 2012)
- Pseudopolymorphs of 2,6-diaminopyrimidin-4-one and 2-amino-6-methylpyrimidin-4-one: one or two tautomers present in the same crystal. (Acta Crystallographica Section C-crystal Structure Communications, 2011)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 2-amino-6-methylpyrimidin-4-one
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SMILESCC1=CC(=O)N=C(N1)N
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InChIKeyKWXIPEYKZKIAKR-UHFFFAOYSA-N
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