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 941289-27-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This chiral piperidine derivative features a carbamate-protected amine and a sterically hindered tert-butyl group, enabling stable incorporation into peptide synthesis workflows. The (3S) stereochemistry ensures high diastereoselectivity in coupling reactions, while the pendant carboxylic acid facilitates efficient conjugation.
(3S)-1-[(1,1-Dimethylethoxy)carbonyl]-3-piperidineacetic acid serves as a stereochemically defined building block for the synthesis of bioactive piperidine derivatives. Its Cbz-protected amine and carboxylic acid functionality enable efficient coupling reactions and orthogonal functional group manipulation. The compound exhibits excellent bench stability and facilitates straightforward purification, making it well-suited for iterative medicinal chemistry campaigns and API intermediate development.
|
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: