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 1175919-93-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
(S)-3-(3-(Allyloxy)phenyl)-2-((tert-butoxycarbonyl)amino)propanoic acid features a chiral center and a protected amine, enabling direct incorporation into peptide synthesis. The allyloxy group provides a handle for orthogonal functionalization, while the tert-butoxycarbonyl moiety ensures stability during handling and storage under standard conditions.
(S)-3-(3-(Allyloxy)phenyl)-2-((tert-butoxycarbonyl)amino)propanoic acid serves as a valuable chiral building block for the synthesis of bioactive heterocycles and peptide-like scaffolds. The allyloxy group enables efficient post-functionalization via click chemistry or transition-metal-catalyzed coupling, while the Boc-protected amine offers orthogonal handling and stability during multi-step syntheses. Bench-stable and readily purified, this compound facilitates scalable access to complex molecular architectures in medicinal chemistry and process development 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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: