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 883987-72-2
| Size |
|
Price | Quantity | |||
|---|---|---|---|---|---|---|
|
* Please select Quantity before adding items. |
||||||
Methyl 3-fluoro-5-nitrobenzoate features a fluorine atom at the meta position and a nitro group at the para position relative to the ester, creating a highly electron-deficient aromatic ring. This combination enhances reactivity in nucleophilic aromatic substitution and enables direct functionalization under mild conditions. The molecule exhibits excellent stability and solubility in common organic solvents, facilitating use in synthetic transformations.
Methyl 3-fluoro-5-nitrobenzoate serves as a versatile building block in medicinal chemistry and agrochemical synthesis, enabling direct functionalization at the aromatic ring due to the orthogonal reactivity of the fluorine and nitro groups. Its bench-stable nature and compatibility with palladium-catalyzed cross-coupling reactions facilitate efficient C–C bond formation. The ester group allows for selective reduction or hydrolysis, offering access to key intermediates for heterocyclic scaffolds and API candidates.
|
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: