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 320-98-9
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
5-Fluoro-2-nitrobenzoic acid features a fluorine atom at the meta position relative to a nitro group, creating a strongly electron-deficient aromatic ring. This configuration enhances reactivity in nucleophilic aromatic substitution and facilitates conjugation in synthetic intermediates. The carboxylic acid functionality enables direct coupling reactions and salt formation for improved solubility.
5-Fluoro-2-nitrobenzoic acid serves as a versatile building block for nitroarene functionalization and heterocycle synthesis, enabling efficient derivatization via nucleophilic aromatic substitution. Its ortho-nitro and meta-fluoro substituents provide orthogonal reactivity for sequential transformations, while the carboxylic acid group supports direct coupling or salt formation. Bench-stable and compatible with standard purification methods, it facilitates streamlined access to complex scaffolds in medicinal chemistry and agrochemical research.
|
GHS Pictogram :
|
GHS No : GHS07
|
|
Signal Word : Warning
|
UN#: N/A
|
|
Class : N/A
|
Packing Group : N/A
|
|
Hazard Statements : H315-H319-H335
|
|
|
Precautionary Statements : P261-P264-P271-P280-P302+P352-P304+P340-P362+P364-P405-P501
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
|
Upload Pictures
|
|
Lot numbers can be found on the outside label of a product: