10472-88-5 | 2-Bromo-4-fluoro-6-nitroaniline

Packsize	Purity	Availability	Price	Discounted Price
1g	98%	in stock	$5.00	$4.00
5g	98%	in stock	$15.00	$11.00
10g	98%	in stock	$18.00	$13.00

Description

• Catalog Number: AB61373
• Chemical Name: 2-Bromo-4-fluoro-6-nitroaniline
• CAS Number: 10472-88-5
• Molecular Formula: C6H4BrFN2O2
• Molecular Weight: 235.0106
• MDL Number: MFCD07779528
• SMILES: Fc1cc(Br)c(c(c1)[N+](=O)[O-])N
• NSC Number: 157607

Computed Properties

• Complexity: 187
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 12
• Hydrogen Bond Acceptor Count: 4
• Hydrogen Bond Donor Count: 1
• XLogP3: 2.4

Upstream Synthesis Route

2-Bromo-4-fluoro-6-nitroaniline is a versatile compound widely used in chemical synthesis due to its unique properties and reactivity. This compound serves as a valuable building block for the synthesis of various pharmaceuticals, agrochemicals, and other fine chemicals. In particular, the presence of both nitro and amino groups in its structure allows for multiple functionalization pathways, enabling the creation of complex organic molecules with specific properties.One key application of 2-Bromo-4-fluoro-6-nitroaniline is in the preparation of heterocyclic compounds, which are essential scaffolds in drug discovery and materials science. By utilizing the versatility of this compound, chemists can introduce diverse substituents and functional groups to tailor the properties of the final molecule. Additionally, the bromo and fluoro substituents present in 2-Bromo-4-fluoro-6-nitroaniline can participate in cross-coupling reactions, enabling the formation of carbon-carbon and carbon-heteroatom bonds with high selectivity.Furthermore, the unique reactivity of 2-Bromo-4-fluoro-6-nitroaniline allows for the selective modification of aromatic systems, leading to the synthesis of highly functionalized aromatic compounds. This versatility makes it a valuable tool for chemists working in the fields of medicinal chemistry, materials science, and agrochemical development.