2-FLUORO-3-NITROBENZOIC ACID CAS 317-46-4

Synonym(s):
2-Fluoro-3-nitrobenzoic acid 99%
3-Carboxy-2-fluoronitrobenzene
3-Pyridinecarboxylic acid, 4-aMino-

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Product Introduction

Product Introduction

Product Name	2-Fluoro-3-nitrobenzoic acid
Product Description	Off-white to white powder
CAS Number	317-46-4
Purity	≥99%
Total impurity	≤1%
Single impurity	≤0.5%
Assay	≥98%
Water	≤0.2%
Molecular Formula	C7H4FNO4
Molecular Weight	185.11
Retest period	12 months
Storage Condition	Store at room temperature
COA/ROS/MSDS/MOA	Provided

Chemical Name

2-Fluoro-3-nitrobenzoic acid

The CAS number for 2-Fluoro-3-nitrobenzoic acid is 317-46-4

The Molecular Formula of 2-Fluoro-3-nitrobenzoic acid is C7H4FNO4

Keywords

Product core characteristics and mechanism of action:
The value of 2-fluoro-3-nitrobenzoic acid mainly stems from the three key functional groups integrated in its molecular structure, making it a "multifunctional reaction building block":
Carboxyl group (-COOH): It can undergo various reactions such as esterification and amide formation, and is a key site for connecting other molecular fragments.
Fluorine atom (F): It has a strong electron-withdrawing effect, which significantly improves the lipid solubility, stability, and biological activity of the molecule. It is a common strategy for introducing fluorine atoms in the design of medicines and pesticides. Nitro (-NO₂): Also a strong electron-withdrawing group, and it can be readily reduced to amine (-NH₂), thereby introducing a wider variety of functional groups and enabling the construction of complex molecules.

APPLICATION

Main application areas	Brief introduction to specific uses	Key features/examples
Pesticide Field	As a key intermediate in the synthesis of novel and highly effective insecticides.	It is used to synthesize diamide insecticides such as bromoxynil and cyprofen.
Pharmaceutical Field	As an important pharmaceutical intermediate, it is used to construct drug molecular skeletons.	Its structure (carboxyl, fluorine, and nitro groups) can optimize drug activity and metabolic properties. It is commonly used as an intermediate in the synthesis of kinase inhibitors, antibacterial agents, etc.
Other fields	As an intermediate in organic synthesis, it is used in materials science (such as liquid crystals and organic optoelectronic materials) and chemical research.	The strong electron-withdrawing effect of fluorine atoms and nitro groups can modulate material properties.