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 723308-59-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This chiral piperidine derivative features a tert-butyl carbamate-protected amine and a methyl group at the 3-position, enabling selective functionalization in asymmetric synthesis. The (3S,4S) stereochemistry ensures predictable stereoselective outcomes in medicinal chemistry applications.
(3S,4S)-tert-Butyl 4-amino-3-methylpiperidine-1-carboxylate serves as a stereochemically defined chiral building block for the synthesis of bioactive piperidine derivatives. Its tert-butyl carbamate group provides excellent bench stability and facilitates straightforward deprotection under mild acidic conditions. The 4-amino functionality enables direct incorporation into diverse coupling reactions, while the 3-methyl substituent enhances conformational rigidity—ideal for constructing pharmaceutically relevant scaffolds in medicinal chemistry 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-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: