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 494194-61-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2,4-Dibromo-5-methylpyrimidine features a sterically accessible pyrimidine core bearing two bromine substituents and a methyl group at the 5-position. This configuration enables direct functionalization in cross-coupling reactions, delivering substituted heterocycles with high regiocontrol. The compound exhibits bench-stable handling and compatibility with palladium-catalyzed transformations under standard conditions.
2,4-Dibromo-5-methylpyrimidine serves as a versatile building block in heterocyclic synthesis, enabling efficient palladium-catalyzed cross-coupling reactions. Its bromine substituents at C2 and C4 positions offer high reactivity in Suzuki, Stille, and Negishi couplings, while the methyl group at C5 enhances stability and solubility. The compound exhibits excellent bench stability and facilitates rapid access to substituted pyrimidine scaffolds relevant to medicinal chemistry and agrochemical development.
|
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: