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 219640-94-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This fluorenylmethoxycarbonyl-protected amino acid derivative features a benzyl side chain with a carboxylic acid group, enabling straightforward incorporation into peptide synthesis workflows. The C-terminal functionality supports efficient coupling reactions under standard conditions, while the fluorenylmethoxycarbonyl group provides robust protection and clean deprotection.
2-(((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)methyl)benzoic acid serves as a robust, bench-stable amino acid derivative enabling efficient peptide synthesis. The Fmoc group provides orthogonal protection for amines with high stability under basic conditions and facile removal via mild acidolysis. The benzoic acid side chain offers a versatile handle for further functionalization, including amide coupling or derivatization, making it ideal for constructing complex peptide scaffolds and bioactive molecules in medicinal chemistry 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: