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 6319-40-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-Bromo-3-nitrobenzoic acid features a bromine substituent and a nitro group positioned ortho to each other on the aromatic ring, creating a highly electron-deficient platform. This configuration enables direct coupling in cross-coupling reactions and facilitates functionalization in pharmaceutical intermediates. The carboxylic acid moiety provides a handle for derivatization under standard conditions.
4-Bromo-3-nitrobenzoic acid serves as a versatile building block for the synthesis of pharmaceutical intermediates and functionalized heterocycles. Its orthogonal reactivity—combining a bromine handle for palladium-catalyzed cross-coupling with a nitro group amenable to reduction and subsequent cyclization—enables efficient access to complex scaffolds. The carboxylic acid functionality supports direct derivatization or salt formation, enhancing solubility and purification. Bench-stable and readily available, it facilitates robust, scalable synthesis workflows in medicinal chemistry and process development.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302
|
|
|
Precautionary Statements : P264-P270-P330-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: