385-02-4 | 2-Fluoro-6-nitrobenzoic acid

Packsize	Purity	Availability	Price	Discounted Price
5g	98%	in stock	$9.00	$7.00
10g	98%	in stock	$11.00	$8.00
25g	98%	in stock	$14.00	$10.00

Description

• Catalog Number: AB44071
• Chemical Name: 2-Fluoro-6-nitrobenzoic acid
• CAS Number: 385-02-4
• Molecular Formula: C7H4FNO4
• Molecular Weight: 185.1094
• MDL Number: MFCD01862079
• SMILES: [O-][N+](=O)c1cccc(c1C(=O)O)F

Computed Properties

• Complexity: 227
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 13
• Hydrogen Bond Acceptor Count: 5
• Hydrogen Bond Donor Count: 1
• Rotatable Bond Count: 1
• XLogP3: 1

Upstream Synthesis Route

2-Fluoro-6-nitrobenzoic acid, a versatile intermediate in chemical synthesis, plays a crucial role in the development of pharmaceuticals and agrochemicals. As a fluorinated aromatic compound, it exhibits unique reactivity and selectivity, making it a valuable building block in organic chemistry.In chemical synthesis, 2-Fluoro-6-nitrobenzoic acid is commonly employed as a key starting material for the preparation of various biologically active molecules. Its functional groups enable it to participate in a wide range of reactions, such as nitration, halogenation, and coupling reactions, leading to the formation of complex structures with desired properties.One prominent application of this compound is its use in medicinal chemistry for the synthesis of fluorinated pharmaceuticals. The incorporation of fluorine atoms into drug molecules can enhance their biological activity, metabolic stability, and pharmacokinetic properties. By introducing 2-Fluoro-6-nitrobenzoic acid into a drug synthesis pathway, researchers can modulate the drug's interactions with biological targets, improving its efficacy and reducing potential side effects.Furthermore, 2-Fluoro-6-nitrobenzoic acid serves as a valuable tool in agrochemical research for designing novel pesticides and herbicides. The introduction of fluorine substituents can impart unique characteristics to agrochemical compounds, such as increased resistance to degradation and enhanced bioavailability. By utilizing this compound in the synthesis of agricultural products, scientists can develop more effective and environmentally friendly solutions for pest control and crop protection.Overall, the strategic incorporation of 2-Fluoro-6-nitrobenzoic acid in chemical synthesis unlocks a plethora of possibilities for creating diverse and advanced organic molecules with applications in pharmaceuticals, agrochemicals, and materials science. Its versatility and reactivity make it a valuable asset in the toolbox of synthetic chemists seeking to innovate and push the boundaries of molecular design.