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 685103-98-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)isoquinoline features a boronate handle integrated into an isoquinoline scaffold, enabling direct coupling in Suzuki-Miyaura reactions. The tetramethyl-substituted dioxaborolane enhances stability and reactivity under standard conditions. This bench-stable building block facilitates efficient access to biologically relevant heterocyclic architectures.
4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)isoquinoline serves as a versatile boronate building block for Suzuki-Miyaura cross-coupling reactions. The isoquinoline core provides a rigid, electron-deficient heterocyclic scaffold with established utility in medicinal chemistry and materials science. The pinacol boronate group ensures excellent bench stability, facilitates easy purification, and enables broad functional group tolerance across diverse coupling partners.
|
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: