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 313342-22-2
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This sulfonamide features a chiral diphenylethylamine scaffold paired with a trifluoromethyl-rich benzene ring, delivering enhanced metabolic stability and lipophilic character. The electron-deficient aryl group facilitates targeted interactions in medicinal chemistry applications, while the primary amine enables straightforward derivatization.
N-[(1S,2S)-2-Amino-1,2-diphenylethyl]-3,5-bis(trifluoromethyl)benzenesulfonamide serves as a chiral sulfonamide building block for medicinal chemistry and catalyst development. The diphenylmethyl amine moiety provides steric bulk and conformational rigidity, while the electron-deficient 3,5-bis(trifluoromethyl)benzenesulfonyl group enhances metabolic stability and modulates solubility. This scaffold enables efficient functionalization via standard amide coupling and sulfonamide derivatization protocols, offering robust performance in high-throughput synthesis workflows.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H312-H332
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P363-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: