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 40741-46-6
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
6-Chloro-3-pyridinesulfonamide features a chlorine-substituted pyridine ring paired with a sulfonamide group, delivering enhanced electron-withdrawing character and improved solubility in polar solvents. This combination enables robust participation in transition metal-catalyzed coupling reactions and facilitates incorporation into bioactive scaffolds requiring precise electronic tuning and metabolic stability.
6-Chloro-3-pyridinesulfonamide serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the 6-position via palladium-catalyzed cross-coupling reactions. Its sulfonamide group provides enhanced solubility and hydrogen-bonding capacity, while the chloropyridine moiety offers predictable reactivity in nucleophilic substitution and transition-metal-catalyzed transformations. The compound exhibits excellent bench stability and facilitates rapid access to diverse heterocyclic scaffolds relevant to kinase inhibitor and CNS-targeted drug discovery programs.
|
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: