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 24623-38-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
1,3-Dichloro-5-methoxyisoquinoline features a sterically hindered isoquinoline core with electron-withdrawing chlorines at positions 1 and 3, enhancing electrophilicity for targeted couplings. The para-methoxy substituent stabilizes the aromatic system while improving solubility in polar organic media. This scaffold enables efficient integration into bioactive molecule frameworks through palladium-catalyzed cross-coupling reactions under standard conditions.
1,3-Dichloro-5-methoxyisoquinoline serves as a versatile building block in medicinal chemistry, enabling regioselective functionalization at the C-7 position via palladium-catalyzed cross-coupling. The electron-withdrawing chlorides and methoxy group provide orthogonal reactivity, enhancing compatibility with diverse nucleophiles. Bench-stable and readily purified, it facilitates efficient access to substituted isoquinoline scaffolds relevant to kinase inhibitors and CNS-targeted therapeutics.
|
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: