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 2864417-86-5
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Chloro-3-fluoro-6-methyl-4-pyridinamine features a trifunctional pyridine core with orthogonal reactivity, enabling direct incorporation into diverse heterocyclic scaffolds. The electron-deficient ring facilitates nucleophilic substitution, while the methyl group provides a handle for further functionalization. This bench-stable intermediate demonstrates excellent compatibility in transition-metal-catalyzed coupling processes and is particularly suited for synthesizing bioactive nitrogen-containing architectures.
2-Chloro-3-fluoro-6-methyl-4-pyridinamine serves as a versatile building block for heterocyclic synthesis, enabling efficient access to substituted pyridine scaffolds relevant in medicinal chemistry. Its orthogonal halogen and amine functionalities facilitate sequential coupling reactions, including Suzuki-Miyaura and Buchwald-Hartwig transformations. The compound exhibits good bench stability and is compatible with standard purification protocols, making it well-suited for iterative synthetic workflows in API development.
|
GHS Pictogram :
N/A
|
GHS No : N/A
|
|
Signal Word : N/A
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : N/A
|
|
|
Precautionary Statements : N/A
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: