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 289889-03-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This protected amino acid derivative features a benzylated amine group flanked by a tert-butoxycarbonyl (Boc) protecting group and a carboxylic acid terminus. Designed for peptide synthesis, it integrates seamlessly into solid-phase workflows, offering stable handling and selective deprotection under mild acidic conditions.
3-{Benzyl[(tert-butoxy)carbonyl]amino}propanoic acid serves as a versatile building block for the synthesis of bioactive peptides and heterocyclic scaffolds. The Boc-protected amino group enables orthogonal handling in multi-step syntheses, while the pendant benzyl moiety offers structural rigidity and potential for further functionalization. This compound exhibits excellent bench stability, facilitates straightforward purification via standard chromatographic methods, and participates reliably in amide coupling and reduction reactions within established peptide chemistry 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: