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 54151-74-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Bromo-4-phenylpyridine features a bromine atom at the 2-position and a phenyl group at the 4-position of the pyridine ring, enabling efficient coupling in palladium-catalyzed cross-coupling reactions. This electron-deficient heterocycle offers high reactivity and stability under standard conditions, facilitating the synthesis of complex biaryl architectures in medicinal chemistry and materials science applications.
2-Bromo-4-phenylpyridine serves as a versatile building block in transition-metal-catalyzed cross-coupling reactions, enabling efficient C–C bond formation under standard Suzuki, Stille, and Negishi conditions. Its phenyl-substituted pyridine framework provides enhanced stability and favorable electronic properties for late-stage functionalization in medicinal chemistry and materials science applications. The bromine handle offers high reactivity with palladium catalysts while maintaining bench stability and compatibility with common protecting groups.
|
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: