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 1062174-44-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
This boronate-functionalized indoline integrates seamlessly into Suzuki-Miyaura coupling reactions under standard conditions. The tetramethylcyclopentadienone-derived boronate moiety ensures excellent stability and compatibility with diverse reaction partners, enabling efficient C–C bond formation in complex molecule synthesis.
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 tetramethylboronate group enables efficient coupling with aryl and heteroaryl halides under mild conditions, while the indoline scaffold provides a stable, bench-accessible platform for constructing biologically relevant nitrogen-containing heterocycles. Functional group tolerance and ease of purification make it well-suited for iterative synthesis in medicinal chemistry and process development.
|
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: