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 2252-37-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Bromo-6-fluorobenzoic acid features a strategically positioned bromine and fluorine substituent on the aromatic ring, enabling selective functionalization in pharmaceutical synthesis. The carboxylic acid group provides a reactive handle for coupling reactions, while the electron-withdrawing halogens enhance regioselectivity. This compound serves as a key building block for bioactive molecules requiring halogenated aromatic scaffolds.
2-Bromo-6-fluorobenzoic acid serves as a valuable building block for the synthesis of fluorinated aromatic scaffolds in medicinal chemistry and agrochemical research. Its ortho-bromine and para-fluorine substituents enable selective cross-coupling reactions, including Suzuki and Stille couplings, while the carboxylic acid group provides a handle for amide formation, esterification, or further functionalization. The compound exhibits good bench stability and facilitates straightforward purification by recrystallization, making it well-suited for scalable synthesis workflows.
|
GHS Pictogram :
|
GHS No : GHS06
|
|
Signal Word : Danger
|
UN#: 2811
|
|
Class : 6.1
|
Packing Group : Ⅲ
|
|
Hazard Statements : H301-H319
|
|
|
Precautionary Statements : P264-P270-P330-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: