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 194668-49-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
tert-Butyl 4-((5-bromopyridin-2-yl)oxy)piperidine-1-carboxylate is a bench-stable, moisture-tolerant building block featuring a brominated pyridine handle and a protected piperidine scaffold. The para-bromo group enables direct cross-coupling reactions, while the tert-butoxycarbonyl moiety provides orthogonal protection for amine functionalization. This structure facilitates rapid access to bioactive heterocycles in medicinal chemistry workflows.
tert-Butyl 4-((5-bromopyridin-2-yl)oxy)piperidine-1-carboxylate serves as a versatile building block for the synthesis of functionalized piperidine derivatives. The bromopyridine moiety enables palladium-catalyzed cross-coupling reactions, while the tert-butyl carbamate group provides stability and facilitates selective deprotection under mild acidic conditions. Its bench-stable nature and compatibility with diverse reaction conditions make it ideal for constructing complex heterocyclic scaffolds in medicinal chemistry and process development workflows.
|
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-P330-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: