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 1209458-16-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-Bromo-N-methyl-2-pyrimidinamine features a bromine substituent at the 4-position and a methylamino group at nitrogen-2, creating a versatile scaffold for medicinal chemistry. The electron-deficient pyrimidine core enables efficient coupling reactions, while the N-methyl group enhances metabolic stability and membrane permeability. This compound serves as a key intermediate in the synthesis of kinase inhibitors and antiviral agents.
4-Bromo-N-methyl-2-pyrimidinamine serves as a versatile building block in medicinal chemistry, enabling palladium-catalyzed cross-coupling reactions due to its reactive bromine and amine functionalities. The N-methyl group enhances metabolic stability while maintaining compatibility with standard coupling protocols. Its pyrimidine core provides a scaffold for constructing bioactive heterocycles, offering bench-stable, easily purified reagents ideal for iterative synthesis workflows in API 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: