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 178876-83-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Methyl 6-amino-3-bromopicolinate features a brominated pyridine core with complementary amino and ester functionalities, enabling direct incorporation into heterocyclic scaffolds. The para-positioned bromine facilitates palladium-catalyzed cross-coupling, while the ortho-amino group offers nucleophilic reactivity for derivatization under mild conditions. This bench-stable intermediate supports efficient access to bioactive picolinate derivatives in medicinal chemistry campaigns.
Methyl 6-amino-3-bromopicolinate serves as a versatile building block in medicinal chemistry, enabling direct functionalization at the amino and bromo positions. Its stability under standard reaction conditions facilitates Suzuki-Miyaura couplings and nucleophilic substitutions, while the ester group permits selective reduction or hydrolysis. The molecule functions as a key intermediate for heterocyclic scaffolds and API precursors in drug discovery workflows.
|
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: