| Weight | 174.587 g/mol |
|---|---|
| Formula | C6H7ClN2O2 |
| Hydrogen Acceptors | 4 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 1 |
| Rotatable Bonds | 2 |
4-Chloro-2,6-dimethoxypyrimidine (6320-15-6)
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- Rate Acceleration of Nucleophilic Substitution of 2-Chloro-4,6-dimethoxypyrimidine by Sulfinate Catalysis (Tetrahedron, 2000)
- Carbonylation of 2-chloro-4,6-dimethoxypyrimidine and 2-(chloromethy)-4,6-dimethoxypyrimidine (Tetrahedron, 1999)
- [Studies on the synthesis of sulfanilamide derivatives. I. Reaction of 6-chloro-2,4-dimethoxypyrimidine with sodium amide in liquid ammonia]. (Yakugaku Zasshi-journal of The Pharmaceutical Society of Japan, 1962)
- Electronic and vibrational spectra of 2,4,6-trichloro- and 6-chloro-2,4-dimethoxypyrimidine (Journal of Chemical Sciences, 1986)
- Zeeman effect of NQR in 4,6-dichloropyrimidine and 6-chloro 2,4-dimethoxypyrimidine (Pramana, 1979)
- Research Progress of Synthesis of 2-chloro-4,6-dimethoxypyrimidine as Pyrimidylsalicylate Herbicides (Journal of Huaihua University, 2009)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCOC1=CC(=NC(=N1)OC)Cl
-
InChIKeyJHNRTJRDRWKAIW-UHFFFAOYSA-N
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