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 100949-34-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
6-Bromo-8-chloro-4(3H)-quinazolinone features a fused bicyclic core with strategically positioned halogen substituents, enabling direct functionalization in transition-metal-catalyzed cross-coupling reactions. The electron-deficient quinazolinone scaffold supports efficient incorporation into bioactive molecule frameworks, particularly in kinase inhibitor development and medicinal chemistry lead optimization.
6-Bromo-8-chloro-4(3H)-quinazolinone serves as a versatile building block for the synthesis of substituted quinazolinones, enabling efficient transition-metal-catalyzed cross-coupling reactions. Its dual halogen functionality offers orthogonal reactivity for sequential derivatization, while its bench-stable nature and compatibility with common reaction conditions facilitate straightforward purification and integration into medicinal chemistry campaigns.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H315-H319
|
|
|
Precautionary Statements : P264-P280-P302+P352-P362+P364
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: