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 2228368-99-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This difluorinated acetic acid derivative features a tert-butoxycarbonyl-protected aniline moiety, enabling straightforward incorporation into peptide synthesis workflows. The electron-withdrawing fluorine atoms enhance stability and modulate reactivity, while the Boc group ensures compatibility with standard deprotection protocols.
2-(4-((tert-Butoxycarbonyl)amino)phenyl)-2,2-difluoroacetic acid serves as a versatile building block for fluoroaromatic peptide mimetics and heterocyclic scaffolds. The difluoromethyl group enhances metabolic stability and modulates pKa, while the Boc-protected amine enables orthogonal functionalization. This compound exhibits excellent bench stability, facilitates straightforward purification via standard chromatography, and participates reliably in coupling reactions, making it well-suited for medicinal chemistry campaigns targeting CNS and oncology therapeutics.
|
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: