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 1114560-76-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-Bromo-2-methylpyrimidine serves as a key heterocyclic scaffold in medicinal chemistry, offering a reactive bromine handle for cross-coupling and a methyl group enabling strategic electronic modulation. This bench-stable building block facilitates efficient access to diverse pyrimidine-based architectures through palladium-catalyzed transformations and nucleophilic substitutions.
4-Bromo-2-methylpyrimidine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions for the construction of biaryl and heteroaryl scaffolds. The bromine atom facilitates efficient functionalization under standard Suzuki, Stille, or Negishi conditions, while the methyl group enhances solubility and modulates electronic properties. Bench-stable and readily purified by recrystallization, it functions reliably in multi-step syntheses of kinase inhibitors and other pharmaceutical 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: