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 204688-61-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This chiral building block features a protected pyrrolidine ring fused to an acetic acid side chain, enabling direct incorporation into peptidomimetics and bioactive scaffolds. The tert-butoxycarbonyl group provides stability during synthesis, while the (S)-configuration ensures stereochemical fidelity in downstream applications.
(S)-2-(1-(tert-butoxycarbonyl)pyrrolidin-3-yl)acetic acid serves as a versatile chiral building block for the synthesis of pyrrolidine-containing pharmaceuticals and natural products. The protected pyrrolidine moiety enables efficient incorporation into complex scaffolds, while the pendant carboxylic acid facilitates coupling reactions. This compound exhibits excellent bench stability and is compatible with standard peptide coupling and reductive amination protocols, making it ideal for medicinal chemistry applications requiring stereocontrolled construction of nitrogen heterocycles.
|
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: