CAS 13106-85-9
:2,4,6-Trimethoxypyrimidine
Description:
2,4,6-Trimethoxypyrimidine is an organic compound characterized by a pyrimidine ring substituted with three methoxy groups at the 2, 4, and 6 positions. Its molecular structure contributes to its unique chemical properties, including its potential solubility in organic solvents and moderate polarity. The presence of methoxy groups enhances its electron-donating ability, which can influence its reactivity and interactions with other chemical species. This compound is often studied for its biological activity, particularly in the context of pharmaceuticals and agrochemicals, where it may exhibit antimicrobial or herbicidal properties. Additionally, 2,4,6-trimethoxypyrimidine can participate in various chemical reactions, such as methylation and substitution, making it a valuable intermediate in synthetic organic chemistry. Safety data indicates that, like many organic compounds, it should be handled with care, using appropriate safety measures to avoid exposure. Overall, its distinctive structure and functional groups make it a compound of interest in both research and industrial applications.
Formula:C7H10N2O3
InChI:InChI=1/C7H10N2O3/c1-10-5-4-6(11-2)9-7(8-5)12-3/h4H,1-3H3
InChI key:InChIKey=RJVAFLZWVUIBOU-UHFFFAOYSA-N
SMILES:O(C)C=1C=C(OC)N=C(OC)N1
Synonyms:- Pyrimidine, 2,4,6-trimethoxy-
- 2,4,6-Trimethoxypyrimidine
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Found 5 products.
2,4,6-Trimethoxypyrimidine
CAS:Formula:C7H10N2O3Purity:>98.0%(GC)Color and Shape:White to Almost white powder to crystalMolecular weight:170.17Pyrimidine, 2,4,6-trimethoxy-
CAS:Formula:C7H10N2O3Purity:98%Color and Shape:SolidMolecular weight:170.16592,4,6-Trimethoxypyrimidine
CAS:Formula:C7H10N2O3Purity:98%Color and Shape:SolidMolecular weight:170.1682,4,6-Trimethoxy-pyrimidine
CAS:Controlled Product<p>2,4,6-Trimethoxy-pyrimidine is a heterobicyclic compound that contains three methoxy groups. It is a synthetic nucleobase that can be found in the nucleosides uridine and cytidine, as well as in other compounds such as pyrimidines. 2,4,6-Trimethoxy-pyrimidine has been shown to be reactive to nucleophilic solutes and has been used with success in the synthesis of lactams. The isomers of this compound have different efficiencies for reaction with nucleophilic solutes.</p>Purity:Min. 95%




