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 41153-30-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
(S)-2-((tert-Butoxycarbonyl)amino)-3-(4-fluorophenyl)propanoic acid is a chiral building block featuring a bench-stable tert-butoxycarbonyl-protected amine and a para-fluorophenyl group. This configuration enables direct incorporation into peptide synthesis workflows, where the protected amine facilitates selective coupling reactions without racemization. The electron-withdrawing fluorine enhances metabolic stability in downstream bioactive compounds.
(S)-2-((tert-Butoxycarbonyl)amino)-3-(4-fluorophenyl)propanoic acid serves as a key chiral building block for peptide synthesis and medicinal chemistry campaigns. The Boc-protected amino group ensures stability and ease of handling, while the 4-fluorophenyl moiety provides a robust aryl handle for further functionalization. This compound facilitates efficient coupling reactions and demonstrates excellent compatibility with standard amide bond formation protocols.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H315-H319-H335
|
|
|
Precautionary Statements : P260-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: