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 220497-48-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This fluorenylmethoxycarbonyl-protected amino acid derivative features a chiral (S)-configuration and incorporates a brominated phenyl group at the beta position. The Cbz moiety ensures stability during peptide synthesis, while the para-bromophenyl side chain provides a handle for downstream functionalization via cross-coupling reactions.
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-3-(3-bromophenyl)propanoic acid serves as a robust chiral building block for peptide synthesis, offering high stereochemical integrity and facile removal of the Fmoc protecting group under mild basic conditions. The pendant bromophenyl moiety enables subsequent functionalization via cross-coupling reactions, while the Fmoc group ensures excellent bench stability and compatibility with standard solid-phase protocols.
|
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: