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 1209498-47-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
6-Bromo-8-fluoroquinazolin-4-ol features a sterically accessible quinazoline core bearing bromo and fluoro substituents at the 6- and 8-positions, respectively. This electron-deficient scaffold integrates readily into synthetic routes requiring halogen-directed functionalization or metal-catalyzed coupling. The hydroxyl group at C4 enables direct derivatization or hydrogen bonding in target binding interactions. Bench-stable under standard conditions, it serves as a key intermediate for bioactive molecule development.
6-Bromo-8-fluoroquinazolin-4-ol serves as a versatile building block for the synthesis of quinazoline-based pharmaceutical scaffolds. Its well-defined halogen and hydroxyl functionalities enable direct functionalization via palladium-catalyzed cross-coupling and nucleophilic substitution reactions. The molecule exhibits excellent bench stability and facilitates straightforward purification, making it ideal for medicinal chemistry campaigns targeting kinase inhibitors and other bioactive heterocycles.
|
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: