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 1132944-44-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronate-functional indoline integrates readily into Suzuki-Miyaura cross-coupling reactions under standard conditions. The methylsulfonyl group enhances solubility and stability, while the tetramethylborolane moiety enables efficient coupling with aryl and heteroaryl halides. Designed for streamlined synthesis of complex pharmaceutical intermediates.
1-(Methylsulfonyl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)indoline serves as a versatile boronate building block for Suzuki-Miyaura cross-coupling reactions. The indoline core provides a privileged scaffold in medicinal chemistry, while the methylsulfonyl group enhances solubility and metabolic stability. The pinacol boronate moiety ensures excellent bench stability, mild reaction conditions, and broad functional group tolerance, enabling efficient construction of complex heterocyclic architectures and drug-like molecules under standard catalytic protocols.
|
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-P280-P302+P352
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: