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 100570-24-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
(R)-1-(3,4-dimethoxyphenyl)ethan-1-amine features a chiral benzylic amine scaffold with two methoxy groups positioned ortho to the ethylamine chain. This electron-rich aromatic system enhances nucleophilicity and facilitates downstream functionalization in asymmetric synthesis. The (R)-stereoisomer offers predictable stereochemical outcomes in catalytic transformations, particularly in the construction of biologically relevant scaffolds. Bench-stable under standard conditions, it serves as a key building block for pharmaceutical intermediates and ligand development.
(R)-1-(3,4-dimethoxyphenyl)ethan-1-amine serves as a valuable chiral building block in medicinal chemistry, enabling the synthesis of bioactive molecules through established amine functionalization and coupling reactions. Its bench-stable nature, combined with orthogonally protected methoxy groups, facilitates selective transformations in multi-step syntheses. The stereochemical purity supports consistent biological evaluation in CNS-targeted drug discovery programs.
|
GHS Pictogram :
|
GHS No : GHS05,GHS07
|
|
Signal Word : Danger
|
UN#: 2735
|
|
Class : 8
|
Packing Group : Ⅲ
|
|
Hazard Statements : H302-H315-H318
|
|
|
Precautionary Statements : P264-P270-P280-P301+P310-P302+P352-P305+P351+P338-P310-P330-P332+P313-P362+P364-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: