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 4373-72-2
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-(3-Bromophenyl)pyridine features a brominated phenyl ring coupled to a pyridine heterocycle, enabling seamless integration into cross-coupling reactions. This electron-deficient aryl halide serves as a robust scaffold for constructing advanced materials and functional molecules in medicinal chemistry and catalysis.
4-(3-Bromophenyl)pyridine serves as a versatile building block in cross-coupling reactions, enabling efficient construction of biaryl scaffolds under standard Pd-catalyzed conditions. The bromo substituent exhibits high reactivity in Suzuki, Stille, and Negishi couplings, while the pyridine nitrogen provides orthogonal functionality for further derivatization. Its bench-stable crystalline form facilitates handling and purification, making it well-suited for iterative synthesis in medicinal chemistry and materials science applications.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H315-H319
|
|
|
Precautionary Statements : P264-P280-P302+P352-P362
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: