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 177966-63-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Fmoc-D-Phe(4-NO2)-OH features a para-nitro substituted phenylalanine residue with enhanced electron-withdrawing character, enabling precise control in peptide synthesis. The Fmoc group ensures efficient orthogonal protection, while the D-configured backbone facilitates incorporation into non-natural sequences. This derivative offers improved solubility and stability under standard coupling conditions.
Fmoc-D-Phe(4-NO₂)-OH serves as a key building block for the synthesis of D-amino acid-containing peptides, particularly in solid-phase peptide synthesis. The 4-nitrophenyl group provides enhanced electrophilicity for selective derivatization and facilitates purification via UV detection. The Fmoc group ensures orthogonal protection, enabling efficient coupling under standard conditions with minimal racemization. This derivative exhibits excellent bench stability and functional group tolerance, making it ideal for constructing complex peptide architectures and bioactive oligomers.
|
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: