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 122565-29-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
(R)-2-Amino-5,5,5-trifluoropentanoic acid features a chiral α-amino acid scaffold with a trifluoromethyl group at the γ-position, conferring enhanced metabolic stability and membrane permeability. This configuration delivers a potent bioisostere for natural amino acids in peptide-based drug design, enabling incorporation into peptidomimetics where resistance to enzymatic degradation is critical.
(R)-2-Amino-5,5,5-trifluoropentanoic acid serves as a valuable chiral building block in medicinal chemistry, enabling the synthesis of fluorinated amino acid derivatives with enhanced metabolic stability. Its trifluoromethyl group imparts strong electron-withdrawing character and lipophilicity, while the stereogenic center supports enantioselective transformations. The compound exhibits bench stability and facilitates straightforward incorporation into peptide scaffolds and bioactive heterocycles via standard coupling and cyclization protocols.
|
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: