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 108279-89-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Chloro-4,6-dimethoxypyridine features a pyridine core bearing chlorine and two methoxy groups at the 2-, 4-, and 6-positions, creating a uniquely activated heterocyclic scaffold. This electronic configuration enables efficient coupling in cross-coupling reactions and facilitates nucleophilic substitution under mild conditions. The compound demonstrates enhanced stability and solubility in common organic solvents, making it well-suited for use in medicinal chemistry and process development workflows.
2-Chloro-4,6-dimethoxypyridine serves as a versatile building block in medicinal chemistry, enabling efficient C–N and C–C bond formations via palladium-catalyzed cross-coupling. Its ortho-chloro functionality exhibits high reactivity in Suzuki, Stille, and Buchwald–Hartwig reactions, while the dimethoxy substituents enhance solubility and stabilize intermediates. The compound demonstrates excellent bench stability and is readily purified by column chromatography, making it ideal for scalable synthesis of heterocyclic scaffolds and API precursors.
|
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: