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 154590-66-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This oxazolidinone derivative features a chiral center and a piperazinyl-substituted aryl group, delivering enhanced solubility and metabolic stability. The fluorinated phenyl moiety imparts electron-withdrawing character, while the acetamide linkage enables facile conjugation in synthetic workflows. Designed for medicinal chemistry applications, it serves as a scaffold for bioactive molecule development.
(S)-N-((3-(3-Fluoro-4-(piperazin-1-yl)phenyl)-2-oxooxazolidin-5-yl)methyl)acetamide serves as a versatile chiral building block in medicinal chemistry, enabling efficient access to complex heterocyclic scaffolds. Its oxazolidinone core provides excellent stereocontrol and bench stability, while the piperazinyl and fluoroaryl groups offer complementary sites for further functionalization. The acetamide side chain enhances solubility and facilitates purification, making it well-suited for iterative synthesis workflows in API development.
|
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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: