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 1364663-27-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Methyl 4,6-dibromonicotinate features two bromine substituents at the 4- and 6-positions of the nicotinate ring, enabling selective functionalization in heterocyclic synthesis. This electron-deficient scaffold integrates readily into cross-coupling reactions, offering high stability under standard conditions and facilitating access to substituted pyridine derivatives with controlled regiochemistry.
Methyl 4,6-dibromonicotinate serves as a versatile building block for the synthesis of brominated heterocycles and functionalized pyridines. Its dual bromine substituents at the 4- and 6-positions enable sequential cross-coupling reactions, facilitating the construction of complex scaffolds in medicinal chemistry. The methyl ester group offers compatibility with standard transformations, while the compound exhibits good bench stability and ease of purification, making it suitable for iterative synthetic 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: