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 53896-49-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Pyridazine-3-carbonitrile features a nitrogen-rich heterocyclic core paired with a nitrile group at the 3-position, enabling versatile integration into pharmaceutical scaffolds. This electron-deficient pyridazine derivative exhibits enhanced reactivity in nucleophilic substitution and transition-metal-catalyzed coupling reactions, offering efficient access to functionalized heteroaromatics under standard conditions.
Pyridazine-3-carbonitrile serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling efficient construction of nitrogen-containing heterocycles. Its nitrile group facilitates nucleophilic addition and subsequent functionalization, while the electron-deficient pyridazine core supports transition-metal-catalyzed coupling reactions. The compound exhibits good bench stability and compatibility with common protecting group strategies, making it well-suited for multi-step synthetic sequences.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302
|
|
|
Precautionary Statements : P264-P270-P330-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: