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 193693-66-2
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This Fmoc-protected pyrrolidine derivative features a chiral (3S) configuration, enabling stereoselective incorporation into peptide chains. The bulky Fmoc group ensures efficient orthogonal protection, while the pyrrolidine ring imparts conformational rigidity, enhancing structural diversity in peptidomimetic design.
(3S)-Fmoc-1-pyrrolidine-3-carboxylic acid serves as a stereochemically defined building block for the synthesis of peptidomimetics and constrained peptide architectures. The Fmoc group enables efficient solid-phase peptide synthesis, while the pyrrolidine ring provides a rigid, bioactive scaffold with favorable conformational control. Its stability under standard coupling conditions and compatibility with diverse functional groups facilitate reliable incorporation into complex molecular frameworks.
|
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: