Lot numbers can be found on the outside label of a product:
Please log in for operation!
*For research and further manufacturing use only, not for direct human use.
Structure of 37554-70-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Chloro-5-fluoro-4-methoxypyrimidine features a trifunctional pyrimidine core with orthogonal reactivity, enabling selective coupling in heterocyclic synthesis. The electron-deficient ring facilitates nucleophilic substitution at the chloro position, while the methoxy and fluoro groups provide steric and electronic control for downstream functionalization. This bench-stable compound serves as a key intermediate in agrochemical and pharmaceutical development workflows.
2-Chloro-5-fluoro-4-methoxypyrimidine serves as a versatile building block in heterocyclic synthesis, enabling efficient construction of pyrimidine-based scaffolds. Its orthogonal reactivity—where the chlorine and fluorine substituents undergo selective nucleophilic substitution—facilitates the modular introduction of diverse aryl, heteroaryl, and amine functionalities. The methoxy group enhances solubility and stability during handling, while the compound exhibits robust bench stability and compatibility with standard coupling protocols. Widely employed in medicinal chemistry and agrochemical research, it functions as a key intermediate in the synthesis of kinase inhibitors and antiviral agents.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: