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 1015070-56-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
6-Bromoisoquinolin-4-ol features a bromine-substituted isoquinoline core with a phenolic hydroxyl group, enabling direct functionalization in cross-coupling and electrophilic substitution reactions. The electron-deficient aromatic system pairs with the reactive OH moiety to facilitate derivatization under mild conditions. This scaffold delivers structural rigidity and enhanced solubility in polar solvents, supporting efficient incorporation into bioactive molecule libraries and advanced synthetic intermediates.
6-Bromoisoquinolin-4-ol serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the C4 hydroxyl and C6 bromine positions. Its stability under standard reaction conditions facilitates Suzuki-Miyaura coupling, nucleophilic substitution, and Pd-catalyzed cross-coupling transformations. The molecule functions effectively in the synthesis of isoquinoline-based pharmacophores and heterocyclic 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-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: