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 210488-53-2
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
(R)-4-(1-Aminoethyl)benzonitrile features a chiral α-amino nitrile scaffold with a para-cyano group, enabling direct incorporation into asymmetric synthesis. The benzonitrile moiety provides a robust handle for further functionalization, while the (R)-configured aminoethyl side chain ensures high stereoselectivity in downstream transformations. This bench-stable compound serves as a key intermediate in medicinal chemistry and catalyst development.
(R)-4-(1-Aminoethyl)benzonitrile serves as a chiral building block for the synthesis of bioactive molecules, enabling efficient access to enantioselective pharmaceutical intermediates. Its benzonitrile group facilitates diverse transformations including nucleophilic additions and transition-metal-catalyzed couplings, while the (R)-configured aminoethylenic side chain provides stereochemical control in downstream derivatization. The compound exhibits bench stability and compatibility with standard purification methods, making it well-suited for use in medicinal chemistry campaigns requiring high enantiomeric purity and predictable reactivity.
|
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-P330-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: