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 367-25-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2,4-Difluoroaniline features two fluorine atoms at the 2- and 4-positions of the aniline ring, imparting enhanced electron-withdrawing character and improved metabolic stability. This ortho- and para-fluorinated scaffold integrates readily into pharmaceutical intermediates, enabling efficient coupling reactions under mild conditions. The molecule exhibits favorable solubility in common organic solvents and maintains stability during standard bench handling.
2,4-Difluoroaniline serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling direct incorporation of fluorinated aromatic scaffolds. Its ortho- and para-fluorine substituents facilitate subsequent cross-coupling reactions and nucleophilic aromatic substitution, while the primary amine functions as a key handle for derivatization. The compound exhibits good bench stability and is compatible with standard purification methods, making it well-suited for use in multi-step synthetic sequences requiring functional group tolerance and predictable reactivity.
|
GHS Pictogram :
|
GHS No : GHS06
|
|
Signal Word : Danger
|
UN#: 2941
|
|
Class : 6.1
|
Packing Group : Ⅲ
|
|
Hazard Statements : H302-H311-H331
|
|
|
Precautionary Statements : P261-P271-P280-P302+P352-P304+P340-P311-P312-P361-P363-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: