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 1261269-66-2
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2,4,6-Trichloronicotinaldehyde features a highly electron-deficient pyridine ring flanked by three chlorine substituents, enhancing its reactivity in nucleophilic addition processes. This bench-stable aldehyde integrates readily into synthetic scaffolds requiring strong electrophilic character, particularly in the construction of heterocyclic systems and functionalized aromatic compounds under standard conditions.
2,4,6-Trichloronicotinaldehyde serves as a versatile building block in synthetic organic chemistry, enabling efficient access to substituted heterocycles and functionalized pharmaceutical intermediates. Its electron-deficient pyridine core facilitates nucleophilic addition and condensation reactions, while the aldehyde group offers straightforward derivatization via imine formation or reductive amination. The molecule exhibits good bench stability and is compatible with standard purification techniques, making it well-suited for use in iterative synthesis campaigns 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: