| Chemical Name: | Pyrimidine, 4-chloro-6-(chloromethyl)-2-methoxy- |
| CAS Number: | 94170-69-1 |
| Product Number: | AG00IHYE(AGN-PC-02OS4E) |
| Synonyms: | |
| MDL No: | |
| Molecular Formula: | C6H6Cl2N2O |
| Molecular Weight: | 193.0306 |
4-Chloro-6-(chloromethyl)-2-methoxypyrimidine is a key intermediate in organic synthesis, particularly in the field of pharmaceuticals and agrochemicals. Its unique structure allows for versatile reactivity, making it a valuable building block in the creation of various biologically active compounds.One important application of 4-Chloro-6-(chloromethyl)-2-methoxypyrimidine is in the synthesis of heterocyclic compounds. By utilizing the chloromethyl group as a reactive site, chemists can introduce additional functional groups or modify the pyrimidine ring to tailor the properties of the final product. This versatility opens up opportunities for the development of novel molecules with targeted biological activities.Furthermore, the methoxy substituent in 4-Chloro-6-(chloromethyl)-2-methoxypyrimidine can serve as a directing group in transition metal-catalyzed coupling reactions. This enables selective bond formation at specific positions on the pyrimidine ring, allowing for precise control over the molecular structure and properties of the desired compound.In summary, 4-Chloro-6-(chloromethyl)-2-methoxypyrimidine plays a crucial role in chemical synthesis by offering a platform for the construction of complex molecules with potential pharmaceutical or agrochemical applications. Its strategic placement of reactive groups makes it a valuable tool for exploring new synthetic pathways and developing innovative compounds.
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