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 2050-22-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Diethyl pyridine-2,3-dicarboxylate features a pyridine ring flanked by two ester-functionalized carbons, enabling its use in transition-metal-catalyzed cross-coupling reactions. The electron-deficient heterocycle facilitates palladium-mediated C–H activation, while the diester moiety offers synthetic versatility for downstream modifications. This bench-stable reagent integrates efficiently into complex molecule assembly workflows.
Diethyl pyridine-2,3-dicarboxylate serves as a versatile synthon in heterocyclic synthesis, enabling efficient access to substituted pyridine scaffolds via multicomponent reactions and transition-metal-catalyzed couplings. The diester functionality provides orthogonal reactivity for selective transformations, while the pyridine core offers inherent stability and compatibility with standard bench protocols. Its robustness under varied reaction conditions facilitates purification and scale-up, making it a reliable building block for medicinal chemistry and process development workflows.
|
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: