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 101774-33-8
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
3-Chloroisoquinolin-4-ol features a chlorinated isoquinoline core with a phenolic hydroxyl group, offering enhanced reactivity for C–H functionalization and transition metal-catalyzed coupling. The electron-deficient aromatic system pairs well with nucleophilic partners, enabling efficient construction of complex heterocycles under mild conditions. This bench-stable scaffold supports direct derivatization without protective group manipulation.
3-Chloroisoquinolin-4-ol serves as a versatile building block in medicinal chemistry, enabling efficient access to isoquinoline-based scaffolds through palladium-catalyzed cross-coupling reactions. Its chlorine substituent facilitates direct functionalization at the C3 position, while the phenolic hydroxyl group offers orthogonal reactivity for derivatization or protection. The compound exhibits good bench stability and compatibility with standard synthetic workflows, supporting its use in the development of 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
|
|
|
Precautionary Statements : P264-P270-P280-P302+P352-P330-P362-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: