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 915087-24-0
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
2-Fluoro-N-methyl-4-nitrobenzamide features a fluorinated aromatic ring paired with electron-withdrawing nitro and amide functionalities, enabling selective reactivity in cross-coupling and bioconjugation workflows. The N-methyl group enhances metabolic stability and solubility, while the para-nitro substituent facilitates downstream transformations. This compound serves as a robust building block for pharmaceutical intermediates and functionalized materials under standard conditions.
2-Fluoro-N-methyl-4-nitrobenzamide serves as a versatile building block in medicinal chemistry, enabling efficient access to fluorinated heterocycles and bioactive scaffolds. Its orthogonal functional groups—fluorine, nitro, and N-methyl amide—facilitate sequential transformations via nucleophilic aromatic substitution, reduction, and coupling reactions. The compound exhibits good bench stability and is compatible with standard purification methods, making it well-suited for iterative synthesis workflows in API development.
|
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: