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 760207-87-2
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
5-Bromo-2-methoxy-3-methylpyridine features a pyridine core functionalized with bromo, methoxy, and methyl groups at strategic positions, enabling selective cross-coupling and derivatization. The electron-deficient ring facilitates palladium-catalyzed reactions, while the methoxy and methyl substituents enhance solubility and stability under standard conditions. This scaffold serves as a key intermediate in medicinal chemistry for nitrogen-rich heterocycles.
5-Bromo-2-methoxy-3-methylpyridine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its well-defined regiochemistry and stability under standard reaction conditions. The methoxy and methyl groups provide orthogonal functional handles for further derivatization, while the bromo substituent facilitates efficient C–C bond formation. Its bench-stable solid form and predictable reactivity make it ideal for modular synthesis of heterocyclic scaffolds and API intermediates.
|
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: