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 209163-25-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This fluorenylmethoxycarbonyl-protected piperidine derivative features a reactive acetic acid handle for conjugation, enabling efficient incorporation into peptide chains. The Cbz-stabilized piperidinone scaffold enhances solubility and stability during synthetic workflows.
2-(3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-oxopiperidin-1-yl)acetic acid serves as a versatile building block for peptide synthesis, enabling efficient incorporation of piperidine-derived motifs into bioactive scaffolds. The Fmoc-protected amine and carboxylic acid functionalities offer orthogonal reactivity, facilitating coupling reactions under standard conditions. Its bench-stable nature and clean purification profile support reliable use in solid-phase and solution-phase 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: