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 412347-30-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
1-(5-Bromopyridin-3-yl)piperazine features a brominated pyridine moiety linked to a piperazine ring, enabling direct incorporation into bioactive scaffolds. The electron-deficient pyridine facilitates metal-catalyzed coupling reactions, while the piperazine nitrogen atoms serve as versatile handles for derivatization. This compound delivers enhanced solubility and metabolic stability in pharmaceutical intermediates.
1-(5-Bromopyridin-3-yl)piperazine serves as a versatile building block for constructing bioactive heterocycles in medicinal chemistry. The bromine substituent enables reliable Suzuki-Miyaura and Buchwald-Hartwig coupling reactions, facilitating the assembly of complex arylated scaffolds. Its piperazine moiety provides solubility and hydrogen-bonding capacity, enhancing pharmacokinetic properties. Bench-stable and readily purified by chromatography or recrystallization, it functions effectively in multistep syntheses targeting kinase inhibitors and CNS modulators.
|
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: