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 1260596-73-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This fluorenylmethoxycarbonyl-protected chiral amino acid features a para-methoxyphenyl side chain and a stereogenic center, enabling precise incorporation into peptide sequences. The Fmoc group facilitates efficient solid-phase synthesis, while the methoxy-substituted aryl moiety enhances solubility and stability under standard coupling conditions.
(S)-2-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-2-(4-methoxyphenyl)acetic acid serves as a robust chiral building block for peptide synthesis, offering high stability and ease of purification. The Fmoc group enables efficient N-terminal protection with orthogonal deprotection under mild basic conditions. The pendant 4-methoxyphenyl moiety provides structural rigidity and enhanced solubility, facilitating downstream coupling reactions in solid-phase and solution-phase 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-P330-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: