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 69696-37-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
5-Bromo-2,4-dimethylpyrimidine features a bromine substituent at the C5 position flanked by two methyl groups, creating a sterically hindered, electron-deficient pyrimidine core. This configuration enables direct coupling in cross-coupling reactions and facilitates incorporation into pharmaceutical scaffolds requiring halogenated heterocycles.
5-Bromo-2,4-dimethylpyrimidine serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient late-stage functionalization via palladium-catalyzed cross-coupling reactions. The bromine atom at the 5-position exhibits high reactivity in Suzuki, Stille, and Negishi couplings, while the methyl groups at positions 2 and 4 provide steric and electronic modulation. This compound offers excellent bench stability, straightforward purification, and compatibility with diverse functional groups, making it a reliable scaffold for constructing biologically active heterocycles and advanced 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: