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 765948-78-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)isoindolin-1-one features a stable boronate ester integrated with an isoindolin-1-one scaffold, enabling efficient Suzuki-Miyaura coupling. This bench-stable reagent facilitates rapid access to biologically relevant heterocyclic architectures under standard conditions.
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)isoindolin-1-one serves as a versatile boronate building block for palladium-catalyzed cross-coupling reactions. Its isoindolin-1-one core provides a rigid, electron-deficient scaffold suitable for medicinal chemistry applications. The tetramethyl-substituted dioxaborolane enhances stability and minimizes protodeboronation, enabling reliable coupling under standard conditions. Ideal for late-stage functionalization and diversity-oriented synthesis.
|
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: