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 120118-14-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
5-Chloro-4-(p-tolyl)-1H-imidazole-2-carbonitrile features a rigid, electron-deficient imidazole core paired with a para-tolyl substituent and nitrile functionality. This combination enhances π-stacking potential and provides a stable scaffold for transition metal-catalyzed coupling reactions in synthetic methodology development.
5-Chloro-4-(p-tolyl)-1H-imidazole-2-carbonitrile serves as a versatile building block in medicinal chemistry, enabling the construction of bioactive heterocyclic scaffolds. Its electron-deficient imidazole core facilitates palladium-catalyzed cross-coupling reactions, while the nitrile and chloro groups offer orthogonal handles for further functionalization. The compound exhibits good bench stability and is compatible with standard purification methods, making it well-suited for iterative synthesis workflows in API development.
|
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: