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 6264-69-3
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
4-Bromobenzene-1,3-diamine features two amine groups positioned meta to each other on a brominated benzene ring, enabling selective coupling in multistep syntheses. The electron-rich aromatic core facilitates efficient transition-metal-catalyzed transformations, while the bromo substituent serves as a robust handle for further functionalization via cross-coupling reactions. This compound demonstrates stability under standard conditions and compatibility with diverse reaction environments.
4-Bromobenzene-1,3-diamine serves as a versatile building block in medicinal chemistry and materials science, enabling efficient access to functionalized aromatic scaffolds. The ortho-diamine motif facilitates palladium-catalyzed cross-coupling reactions and cyclization processes, while the bromine substituent supports further derivatization via Suzuki-Miyaura or Buchwald-Hartwig coupling. Its bench-stable nature and compatibility with diverse reaction conditions make it a practical choice for constructing complex heterocycles and API intermediates.
|
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-P280-P302+P352
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: