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 390815-41-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
(R)-1-(3,4-Dimethoxyphenyl)ethanamine hydrochloride features a chiral amine core with two methoxy groups enhancing solubility and metabolic stability. This bench-stable derivative serves as a key building block in asymmetric synthesis and bioactive molecule development, offering predictable stereochemical behavior under standard conditions.
(R)-1-(3,4-Dimethoxyphenyl)ethanamine hydrochloride serves as a chiral building block for bioactive molecule synthesis, enabling efficient access to pharmacologically relevant scaffolds. The amine functionality facilitates straightforward derivatization via alkylation, acylation, and coupling reactions. Bench-stable and readily purified by recrystallization or ion-exchange chromatography, it exhibits excellent functional group tolerance in standard synthetic workflows. Its defined stereochemistry ensures consistent enantioselective outcomes in asymmetric synthesis.
|
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: