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 1931107-98-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This fluorenylmethoxycarbonyl-protected serine derivative features a stable, electron-rich fluoren-9-ylmethoxy carbonyl group that enables efficient coupling in peptide synthesis. The O-ethyl and N-methyl substitutions enhance solubility and reduce side reactions, while the protected hydroxyl and amino groups provide orthogonal functionality for sequential derivatization.
N-(((9H-Fluoren-9-yl)methoxy)carbonyl)-O-ethyl-N-methyl-L-serine serves as a versatile, bench-stable amino acid derivative for solid-phase peptide synthesis. Its Fmoc group enables orthogonal protection, while the O-ethyl and N-methyl functionalities provide enhanced solubility and reduced racemization risk during coupling. The molecule facilitates efficient incorporation of modified serine residues into peptide sequences, supporting both manual and automated synthesis workflows with high fidelity and ease of purification.
|
GHS Pictogram :
N/A
|
GHS No : N/A
|
|
Signal Word : N/A
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : N/A
|
|
|
Precautionary Statements : N/A
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: