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 141743-13-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This fluorenylmethoxycarbonyl-protected amino acid derivative features a benzyl-substituted amine handle, enabling efficient solid-phase peptide synthesis. The fluoren-9-ylmethoxycarbonyl group ensures high-yield deprotection under mild conditions, while the benzyl moiety enhances solubility and stability during coupling steps.
2-((((9H-Fluoren-9-yl)methoxy)carbonyl)(benzyl)amino)acetic acid serves as a robust amino acid building block for peptide synthesis, combining the stability of Fmoc protection with benzyl-assisted solubility and orthogonal deprotection. Its structure enables efficient coupling reactions and facilitates purification via standard chromatographic methods, making it well-suited for iterative solid-phase synthesis workflows in medicinal chemistry and protein engineering.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: