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 23100-12-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Chloropyridine-5-carbaldehyde features a pyridine ring bearing both chloro and aldehyde functionalities at adjacent positions, enabling direct integration into heterocyclic synthesis. The electron-deficient aldehyde group facilitates nucleophilic addition reactions, while the chloro substituent serves as a latent handle for further functionalization via cross-coupling or displacement. This bifunctional scaffold supports efficient access to bioactive molecules in medicinal chemistry and materials science.
2-Chloropyridine-5-carbaldehyde serves as a versatile building block in medicinal chemistry and heterocyclic synthesis. Its aldehyde functionality enables efficient imine formation, reductive amination, and Suzuki-Miyaura coupling, while the chloropyridine moiety offers compatibility with palladium-catalyzed cross-couplings. Bench-stable and readily purified by chromatography, it facilitates the construction of complex pyridine-based scaffolds relevant to pharmaceutical development.
|
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: