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 197507-55-4
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
8-Bromo-1,6-naphthyridine-2-carboxylic acid features a fused bicyclic core with complementary electron-deficient character and a bromo substituent at the 8-position. This configuration enables direct functionalization via cross-coupling reactions, while the carboxylic acid group facilitates conjugation or salt formation. The compound exhibits bench-stable handling properties and is well-suited for medicinal chemistry applications requiring rigid, polar heterocyclic scaffolds.
8-Bromo-1,6-naphthyridine-2-carboxylic acid serves as a versatile building block for the synthesis of bioactive heterocycles, particularly in medicinal chemistry and agrochemical development. The bromo group enables palladium-catalyzed cross-coupling reactions, while the carboxylic acid facilitates amide bond formation and derivatization. Its stability under standard reaction conditions and compatibility with diverse functional groups make it well-suited for iterative synthetic strategies and scaffold diversification.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H312-H315-H319-H332-H335
|
|
|
Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P330-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: