| Weight | 140.142 g/mol |
|---|---|
| Formula | C6H8N2O2 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
2,4-Dimethoxypyrimidine (3551-55-1)
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- Relative enthalpies of 1,3-dimethyl-2,4-pyrimidinedione, 2,4-dimethoxypyrimidine, and 4-methoxy-1-methyl-1-2-pyrimidinone: estimation of the relative stabilities of two protomers of uracil (Journal of the American Chemical Society, 1982)
- Vibrational spectroscopy investigation using ab initio and density functional theory analysis on the structure of 2 -amino -4,6 -dimethoxypyrimidine (Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy, 2006)
- Rate Acceleration of Nucleophilic Substitution of 2-Chloro-4,6-dimethoxypyrimidine by Sulfinate Catalysis (Tetrahedron, 2000)
- Palladium-catalysed carbomethoxyvinylation and thienylation of 5-iodo(bromo)-2,4-dimethoxypyrimidine in water (Tetrahedron Letters, 1997)
- Carbonylation of 2-chloro-4,6-dimethoxypyrimidine and 2-(chloromethy)-4,6-dimethoxypyrimidine (Tetrahedron, 1999)
- Nucleic acids components and their analogues. LXVII. The Hilbert-Johnson reaction of protected 2-deoxy-D-ribofuranosyl chlorides with 2,4-dimethoxypyrimidine and its 5-methyl derivative (Collection of Czechoslovak Chemical Communications, 1965)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCOC1=NC(=NC=C1)OC
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InChIKeyKEVRHVMWBKFGLO-UHFFFAOYSA-N
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Similar Compounds
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