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 183673-66-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
1-Boc-piperidine-4-Fmoc-amino-4-carboxylic acid features a bifunctional scaffold integrating a protected piperidine ring with orthogonal handling groups. The Boc group ensures stability during synthesis, while the Fmoc moiety enables efficient, selective deprotection under mild conditions. This dual protection strategy facilitates precise incorporation into peptide chains and complex molecular architectures.
1-Boc-piperidine-4-Fmoc-amino-4-carboxylic acid serves as a versatile bifunctional building block for the synthesis of constrained peptidomimetics and heterocyclic scaffolds. The Boc-protected amine enables orthogonal handling in multi-step syntheses, while the Fmoc group facilitates efficient solid-phase peptide coupling. The carboxylic acid functionality supports direct amidation or esterification, enabling integration into complex molecular architectures with high functional group tolerance and bench stability.
|
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: