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 856211-63-7
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Methyl 6-amino-5-chloronicotinate features a chlorinated pyridine core with complementary amino and ester functionalities, enabling direct incorporation into heterocyclic scaffolds. The para-chloro group enhances electrophilicity for cross-coupling reactions, while the primary amine facilitates derivatization under mild conditions. This bench-stable reagent streamlines synthesis of bioactive nitrogen-containing compounds.
Methyl 6-amino-5-chloronicotinate serves as a versatile building block in medicinal chemistry, enabling the synthesis of substituted pyridine derivatives via standard coupling and cyclization protocols. The amino and chloro groups offer orthogonal reactivity for selective functionalization, while the ester moiety facilitates downstream transformations. Its bench-stable nature and compatibility with common reaction conditions make 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 : H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: