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 206060-42-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Fmoc-Phe(3-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 deprotection under mild basic conditions. This derivative integrates seamlessly into complex sequences, offering improved solubility and stability during solid-phase workflows.
Fmoc-Phe(3-NO₂)-OH serves as a valuable building block for peptide synthesis, enabling the incorporation of meta-nitrophenylalanine into polypeptide chains. The electron-withdrawing nitro group enhances the reactivity of the adjacent aromatic ring, facilitating downstream functionalization via reduction or nucleophilic substitution. Its Fmoc protection ensures compatibility with standard solid-phase peptide synthesis protocols, offering bench stability and ease of purification.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H312-H332
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: