3-Bromo-4-fluoroaniline, 98%
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3-Bromo-4-fluoroaniline, 98%
3-Bromo-4-fluoroaniline, 98%
3-Bromo-4-fluoroaniline, 98%
Thermo Scientific Chemicals

3-Bromo-4-fluoroaniline, 98%

CAS: 656-64-4 | C6H5BrFN | 190.015 g/mol
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25 g
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Catalog number B25610.14
also known as B25610-14
Price (USD)
293.65
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Quantity:
25 g
Request bulk or custom format
Price (USD)
293.65
Online Exclusive
326.00
Save 32.35 (10%)
Each
Add to cart
Chemical Identifiers
CAS656-64-4
IUPAC Name3-bromo-4-fluoroaniline
Molecular FormulaC6H5BrFN
InChI KeyKOWPUNQBGWIERF-UHFFFAOYSA-N
SMILESNC1=CC(Br)=C(F)C=C1
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SpecificationsSpecification SheetSpecification Sheet
FormCrystals or powder or crystalline powder or lumps or fused solid or clear liquid as melt
Assay (GC)≥97.5%
Identification (FTIR)Conforms
Melting Point (clear melt)27.0-34.0?C
Refractive Index1.5925-1.5965 @ 20?C
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3-Bromo-4-fluoroaniline is used in organic synthesis as an intermediate of agrochemicals and active pharmaceutical ingredient.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
3-Bromo-4-fluoroaniline is used in organic synthesis as an intermediate of agrochemicals and active pharmaceutical ingredient.

Solubility
Insoluble in water.

Notes
Incompatible with strong oxidizing agents, strong acids and bases.
RUO – Research Use Only

General References:

  1. Lei, T.; Xia, X.; Wang, J. Y.; Liu, C. J.; Pei, J. Conformation Locked Strong Electron-Deficient Poly(p-Phenylene Vinylene) Derivatives for Ambient-Stable n-Type Field-Effect Transistors: Synthesis, Properties, and Effects of Fluorine Substitution Position. J. Am. Chem. Soc. 2014, 136 (5), 2135-2141.
  2. Patrick, R.; Nagarajan, N. S.; Pan, H.; Saha, S. K.; Rapai, J.; Torlikonda, V.; Panda, M.; Manjunatha, S. G.; Nambiar, S. Understanding of the mass spectrometric fragmentation pathways of a few potentially genotoxic haloaniline isomers in their protonated form by collision-induced dissociation. J. Pharm. Biomed. Anal. 2011, 56 (4), 721-727.