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 205688-13-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This fluorenylmethoxy carbamate derivative features a robust protecting group for primary amines, combining the stability of the 9-fluorenylmethyl (Fmoc) moiety with a para-aminophenyl linker. The carbamate linkage enables efficient deprotection under mild basic conditions, facilitating controlled release during peptide synthesis and enabling clean coupling reactions in biopharmaceutical workflows.
(9H-Fluoren-9-yl)methyl (4-aminophenyl)carbamate serves as a robust amino-protecting group for peptide synthesis and nucleoside derivatization. Its fluorenylmethoxycarbonyl (Fmoc) moiety enables orthogonal deprotection under mild basic conditions, while the para-aminophenyl carbamate functionality offers enhanced stability and compatibility with diverse functional groups. This compound facilitates efficient solid-phase synthesis and simplifies purification through distinct chromatographic behavior.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H315-H319
|
|
|
Precautionary Statements : P264-P280-P302+P352-P362
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: