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 1060811-24-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
6-Bromo-4-chloronicotinaldehyde is a halogenated pyridine aldehyde featuring complementary reactive handles for cross-coupling and functionalization. The para-halogenated scaffold enables efficient Pd-catalyzed transformations, while the aldehyde group serves as a direct anchor for reductive amination or imine formation under mild conditions. This bench-stable reagent integrates seamlessly into synthetic sequences requiring selective installation of electron-deficient heterocyclic motifs.
6-Bromo-4-chloronicotinaldehyde serves as a versatile building block in medicinal chemistry, enabling the construction of heterocyclic scaffolds via palladium-catalyzed cross-coupling and condensation reactions. Its dual halogenation pattern supports sequential functionalization, while the aldehyde group facilitates imine formation and cyclization processes. Bench-stable and readily purified by flash chromatography, it functions efficiently in multi-step syntheses requiring orthogonal reactivity.
|
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: