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 66909-33-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Chloro-5-cyano-3-picoline features a trifunctional pyridine core with chlorine, cyano, and methyl groups positioned for orthogonal reactivity. This electron-deficient heterocycle enables selective coupling in transition-metal-catalyzed transformations. The nitrile moiety enhances solubility in polar solvents while maintaining stability under standard bench conditions.
2-Chloro-5-cyano-3-picoline serves as a versatile building block in medicinal chemistry, enabling efficient construction of heterocyclic scaffolds via palladium-catalyzed cross-coupling reactions. The chloro group facilitates reliable functionalization under standard Suzuki, Stille, or Negishi conditions, while the nitrile moiety provides a handle for downstream transformations such as amide formation or reductive amination. Its bench-stable nature and compatibility with diverse reaction conditions make it well-suited for iterative synthesis campaigns in API development.
|
GHS Pictogram :
|
GHS No : GHS06
|
|
Signal Word : Danger
|
UN#: 3439
|
|
Class : 6.1
|
Packing Group : Ⅲ
|
|
Hazard Statements : H301
|
|
|
Precautionary Statements : P264-P270-P330-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: