1190198-31-2 | 2-Bromo-4-nitro-5-(trifluoromethyl)aniline

Packsize	Purity	Availability	Price	Discounted Price
100mg	98%	in stock	$6.00	$4.00
250mg	98%	in stock	$8.00	$6.00
1g	98%	in stock	$23.00	$17.00
5g	98%	in stock	$80.00	$56.00

Description

• Catalog Number: AI68369
• Chemical Name: 2-Bromo-4-nitro-5-(trifluoromethyl)aniline
• CAS Number: 1190198-31-2
• Molecular Formula: C7H4BrF3N2O2
• Molecular Weight: 285.0181
• MDL Number: MFCD12922693
• SMILES: Brc1cc([N+](=O)[O-])c(cc1N)C(F)(F)F

Computed Properties

• Complexity: 256
• Covalently-Bonded Unit Count: 1
• Heavy Atom Count: 15
• Hydrogen Bond Acceptor Count: 6
• Hydrogen Bond Donor Count: 1
• XLogP3: 2.6

Upstream Synthesis Route

2-Bromo-4-nitro-5-(trifluoromethyl)benzenamine is a versatile compound that finds its primary application in chemical synthesis as a valuable building block. With its unique molecular structure, this compound serves as a key intermediate in the synthesis of various pharmaceuticals, agrochemicals, and other fine chemicals. Its incorporation into organic molecules imparts desirable chemical properties and functionalities, making it a valuable tool for synthetic chemists.In the realm of chemical synthesis, 2-Bromo-4-nitro-5-(trifluoromethyl)benzenamine plays a crucial role in the construction of complex molecular architectures. Its ability to participate in various synthetic reactions, such as nucleophilic aromatic substitution, allows for efficient derivatization and functionalization of organic molecules. This compound's trifluoromethyl group, in particular, introduces unique electronic and steric effects that influence the reactivity and selectivity of chemical transformations.Moreover, the presence of both bromo and nitro functionalities in 2-Bromo-4-nitro-5-(trifluoromethyl)benzenamine enables further diversification through cross-coupling reactions and other synthetic methodologies. Chemists leverage these functional groups to introduce additional substituents or build molecular complexity, leading to the development of novel compounds with tailored properties for specific applications.Overall, 2-Bromo-4-nitro-5-(trifluoromethyl)benzenamine's role in chemical synthesis extends beyond a mere building block; it serves as a strategic tool for accessing structurally diverse compounds with potential utility in various fields, including pharmaceuticals, materials science, and agrochemicals.