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 128071-93-2
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2,4-Dibromo-3-methylpyridine features a pyridine core with bromine substituents at the 2 and 4 positions and a methyl group at the 3 position, delivering enhanced reactivity for cross-coupling applications. The electron-deficient aromatic ring enables efficient palladium-catalyzed transformations, while the sterically accessible methyl moiety provides a handle for further functionalization. This bench-stable compound serves as a key building block in the synthesis of bioactive heterocycles and advanced materials.
2,4-Dibromo-3-methylpyridine serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling palladium-catalyzed cross-coupling reactions due to its well-defined halogen reactivity. The methyl group enhances regioselectivity in electrophilic substitutions, while the dibromo substitution pattern facilitates sequential functionalization. Its bench-stable nature and compatibility with standard purification protocols make it ideal for multi-step synthetic sequences requiring precise heterocyclic scaffolding.
|
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-P280-P302+P352
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: