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 73568-41-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2,6-Dichloroquinoline-3-carbaldehyde delivers a rigid, electron-deficient quinoline scaffold bearing two ortho-chloro substituents that enhance electrophilicity at the aldehyde center. This configuration supports efficient coupling reactions in heterocyclic synthesis and enables selective functionalization under mild conditions.
2,6-Dichloroquinoline-3-carbaldehyde serves as a versatile building block in heterocyclic synthesis, enabling efficient access to quinoline-based scaffolds through nucleophilic addition and condensation reactions. Its dual chlorine substituents enhance electrophilicity at the C3 position, facilitating coupling with amines, hydrazines, and other nitrogen nucleophiles under mild conditions. The aldehyde functionality provides a handle for further derivatization, including reductive amination and oxime formation. Bench-stable and readily purified by recrystallization, it functions effectively in medicinal chemistry lead optimization and API intermediate development.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H319
|
|
|
Precautionary Statements : P264-P270-P280-P330-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: