364-76-1 | 4-Fluoro-3-nitroaniline

Packsize	Purity	Availability	Price	Discounted Price
25g	98%	in stock	$11.00	$8.00
100g	98%	in stock	$18.00	$13.00
500g	98%	in stock	$88.00	$62.00

Description

• Catalog Number: AB67504
• Chemical Name: 4-Fluoro-3-nitroaniline
• CAS Number: 364-76-1
• Molecular Formula: C6H5FN2O2
• Molecular Weight: 156.1145
• MDL Number: MFCD00007833
• SMILES: Nc1ccc(c(c1)[N+](=O)[O-])F
• NSC Number: 10293

Computed Properties

• Complexity: 159
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 11
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 1
• XLogP3: 0.8

Upstream Synthesis Route

4-Fluoro-3-nitrobenzenamine, also known as $name$, is a versatile chemical compound widely used in organic synthesis. Primarily, it is employed as a key building block in the production of various pharmaceuticals, agrochemicals, and fine chemicals. The presence of a fluoro group in the molecule imparts unique properties that enhance its reactivity and selectivity in numerous chemical reactions.In chemical synthesis, 4-Fluoro-3-nitrobenzenamine serves as a valuable intermediate in the preparation of biologically active compounds. Its nitro and amino groups can undergo various transformations such as reduction, substitution, and coupling reactions to introduce functional groups at specific positions on the benzene ring. This enables chemists to tailor the molecular structure of target compounds, leading to the development of novel drugs, pesticides, and other advanced materials.Furthermore, the fluoro substituent in 4-Fluoro-3-nitrobenzenamine is particularly advantageous in medicinal chemistry. Fluorinated organic compounds have been found to exhibit improved pharmacokinetic properties, bioavailability, and metabolic stability compared to their non-fluorinated counterparts. Therefore, the strategic incorporation of a fluorine atom in drug design using this compound as a precursor can potentially enhance the therapeutic efficacy and safety profile of the final pharmaceutical products.Overall, the strategic application of 4-Fluoro-3-nitrobenzenamine in chemical synthesis plays a crucial role in the development of innovative molecules with diverse functionalities and applications across the pharmaceutical, agricultural, and materials science industries.