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 2343-25-1
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
1-(2-Amino-5-fluorophenyl)ethanone features a fluorinated aromatic ring paired with a reactive acetamido group, enabling direct integration into pharmaceutical scaffolds. The para-fluoro substitution enhances metabolic stability, while the amino functionality supports facile derivatization under standard conditions. This compound serves as a key intermediate in the synthesis of bioactive molecules targeting neurological and oncological pathways.
1-(2-Amino-5-fluorophenyl)ethanone serves as a versatile building block for the synthesis of fluorinated aromatic scaffolds. Its ortho-amino and fluoro substituents enable directed metalation and facilitate transition-metal-catalyzed coupling reactions. The ketone functionality supports nucleophilic additions and reductive transformations, offering reliable access to substituted anilines and heterocyclic intermediates in medicinal chemistry workflows. Bench-stable and amenable to standard purification methods, it functions effectively in multi-step syntheses requiring functional group compatibility.
|
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-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: