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 1224629-03-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
5-Bromo-1-fluoro-3-methyl-2-nitrobenzene features a strategically positioned nitro group and halogen substituents that enable selective cross-coupling reactions under mild conditions. The electron-deficient aromatic core pairs well with palladium catalysts, while the methyl group enhances solubility and reduces aggregation during synthesis. This compound serves as a key intermediate in the construction of bioactive heterocycles and functionalized materials.
5-Bromo-1-fluoro-3-methyl-2-nitrobenzene serves as a versatile building block for palladium-catalyzed cross-coupling reactions, leveraging orthogonal halogen reactivity. The fluorine and bromine substituents enable sequential functionalization, while the nitro and methyl groups provide defined electronic and steric control. This compound exhibits excellent bench stability and facilitates efficient purification, making it well-suited for the synthesis of complex heterocycles and pharmaceutical intermediates.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H302-H315-H320-H335
|
|
|
Precautionary Statements : P264-P270-P330
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: