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 914610-50-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
N-Cyclopropyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide features a boronate ester group paired with a cyclopropyl-substituted sulfonamide. This stable, moisture-tolerant reagent integrates readily into Suzuki-Miyaura coupling reactions, enabling efficient C–C bond formation under mild conditions. The electron-deficient aryl sulfonamide scaffold enhances reactivity and functional group compatibility in complex molecular architectures.
N-Cyclopropyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzenesulfonamide serves as a stable, bench-ready boronate building block for Suzuki-Miyaura cross-coupling reactions. The sulfonamide group provides enhanced solubility and metabolic stability, while the cyclopropyl substituent offers favorable steric and electronic properties. Its compatibility with diverse reaction conditions enables efficient construction of biaryl scaffolds in medicinal chemistry and materials synthesis.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302
|
|
|
Precautionary Statements : P264-P270-P330-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: