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 19932-87-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
6-Iodo-2(3H)-benzoxazolone features a reactive iodine handle at the 6-position, enabling direct coupling in transition-metal-catalyzed transformations. The benzoxazolone core provides enhanced stability and facilitates incorporation into complex heterocyclic architectures under mild conditions. This compound serves as a robust scaffold for diversification in medicinal chemistry and materials synthesis.
6-Iodo-2(3H)-benzoxazolone serves as a versatile building block in transition-metal-catalyzed cross-coupling reactions, enabling efficient access to functionalized benzoxazolone scaffolds. Its iodine substituent facilitates palladium-catalyzed coupling with arylboranes, alkenylstannanes, and other nucleophiles under standard conditions. The molecule exhibits good bench stability and reacts selectively at the C6 position, offering predictable regiochemistry for downstream synthesis of bioactive heterocycles and pharmaceutical intermediates.
|
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-P330-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: