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 73568-25-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Chloroquinoline-3-carbaldehyde features a chlorinated quinoline core with an aldehyde handle at the 3-position, enabling direct integration into heterocyclic synthesis. The electron-deficient aromatic system enhances reactivity in nucleophilic additions and condensation reactions. This bench-stable compound serves as a key intermediate for pharmaceuticals and functional materials.
2-Chloroquinoline-3-carbaldehyde serves as a versatile building block in medicinal chemistry and heterocyclic synthesis, enabling efficient access to quinoline-based scaffolds. Its aldehyde functionality supports standard transformations including reductive amination, Grignard additions, and Wittig reactions, while the ortho-chloro substituent facilitates palladium-catalyzed coupling processes. The compound exhibits good bench stability and is readily purified by column chromatography, making it well-suited for multi-step synthesis workflows.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: