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 84773-29-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
(S)-2-(Methylamino)-3-phenylpropan-1-ol features a chiral center at the C2 position, delivering enantioselective reactivity in medicinal chemistry applications. The pendant phenyl group imparts aromatic character and π-stacking potential, while the primary alcohol enables derivatization. This configuration supports structural mimicry of biologically active amines, enhancing target engagement in CNS-directed drug discovery.
(S)-2-(Methylamino)-3-phenylpropan-1-ol serves as a key chiral building block in the synthesis of β-arylethanolamine derivatives. Its well-defined stereochemistry enables reliable incorporation into pharmaceutically relevant scaffolds, including adrenergic receptor ligands. The molecule exhibits bench stability, tolerates common functional groups, and facilitates straightforward purification. It functions effectively in amine alkylation, reduction, and coupling reactions, making it a practical intermediate for medicinal chemistry campaigns requiring enantiopure arylalkylamines.
|
GHS Pictogram :
|
GHS No : GHS05
|
|
Signal Word : Danger
|
UN#: 3259
|
|
Class : 8
|
Packing Group : Ⅲ
|
|
Hazard Statements : H314
|
|
|
Precautionary Statements : P260-P264-P280-P301+P330+P331-P304+P340-P363-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: