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 36404-89-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Hydroxynicotinaldehyde features a strategically positioned aldehyde and hydroxyl group on a pyridine ring, enabling versatile coordination in metal complexes and facilitating efficient cyclization reactions. This bench-stable heterocycle integrates readily into synthetic pathways for bioactive scaffolds and functional materials.
2-Hydroxynicotinaldehyde serves as a versatile building block in heterocyclic synthesis, enabling efficient access to quinoline and isoquinoline derivatives via condensation and cyclization protocols. Its dual aldehyde and phenolic hydroxyl functionalities provide orthogonal reactivity for sequential functionalization, while its bench stability facilitates handling in multi-step sequences. The compound functions effectively in transition-metal-catalyzed coupling reactions and is compatible with common protecting group strategies, making it a practical choice for medicinal chemistry and process development workflows.
|
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: