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 2206320-30-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2,4-Dichloro-6-ethoxyquinazoline features a sterically accessible quinazoline core with complementary electron-withdrawing chloro groups and a moisture-tolerant ethoxy substituent. This configuration enables efficient coupling in transition-metal-catalyzed cross-coupling reactions, particularly in the synthesis of bioactive heterocycles and kinase inhibitor scaffolds under standard conditions.
2,4-Dichloro-6-ethoxyquinazoline serves as a versatile building block in medicinal chemistry, enabling efficient construction of quinazoline-based scaffolds through nucleophilic substitution. The dichloro pattern facilitates sequential functionalization at C2 and C4 positions, while the ethoxy group enhances solubility and stability under standard reaction conditions. Its bench-stable nature and compatibility with diverse coupling partners make it ideal for synthesizing 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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: