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D101400

Sigma-Aldrich

2,4-Difluoroaniline

99%

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About This Item

Linear Formula:
F2C6H3NH2
CAS Number:
Molecular Weight:
129.11
Beilstein:
2802556
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

99%

form

liquid

refractive index

n20/D 1.506 (lit.)

bp

170 °C/753 mmHg (lit.)

mp

−7.5 °C (lit.)

density

1.268 g/mL at 25 °C (lit.)

SMILES string

Nc1ccc(F)cc1F

InChI

1S/C6H5F2N/c7-4-1-2-6(9)5(8)3-4/h1-3H,9H2

InChI key

CEPCPXLLFXPZGW-UHFFFAOYSA-N

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Pictograms

Skull and crossbones

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 3 Dermal - Acute Tox. 4 Oral

Storage Class Code

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

WGK

WGK 1

Flash Point(F)

143.6 °F - closed cup

Flash Point(C)

62 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Wei Chih Huang et al.
Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy, 93, 176-179 (2012-04-07)
We applied the two-color resonant two-photon ionization and mass-analyzed threshold ionization techniques to record the vibronic and cation spectra of 2,4-difluoroaniline. The cation spectra were recorded by ionizing via the 0(0), X(1), 6b(1), and 1(1) levels of the electronically excited
Sergey E Korchak et al.
The Journal of chemical physics, 137(9), 094503-094503 (2012-09-11)
Effects of spin-spin interactions on the nuclear magnetic relaxation dispersion (NMRD) of protons were studied in a situation where spin ½ hetero-nuclei are present in the molecule. As in earlier works [K. L. Ivanov, A. V. Yurkovskaya, and H.-M. Vieth
Duoli Guo et al.
AAPS PharmSciTech, 13(2), 661-673 (2012-05-04)
A stability-indicating high-performance liquid chromatography method to quantify 2-(2,4-difluorophenyl)-4,5,6,7-tetrafluoroisoindoline-1,3-dione (NSC-726796) and its three main degradation products was developed. This method was used to investigate its degradation kinetics and mechanism. The reaction follows first-order kinetics and appears to be base catalyzed
Gergely Rácz et al.
Pathology oncology research : POR, 18(3), 579-584 (2011-12-14)
Disinfection of raw water is essential to the production of drinking water. However, by-products of disinfection may exert toxic effects. The potential toxic effects of two of these compounds, 4-ethylbenzaldehyde (EBA) and 2,4-difluoroaniline (DFA) were investigated using the zebrafish (Danio
Junyu Guo et al.
Environmental pollution (Barking, Essex : 1987), 225, 175-183 (2017-04-04)
Trifluoroacetic acid (TFA) in the atmosphere is produced by degradation of hydrochlorofluorocarbons and hydrofluorocarbons. In recent years, TFA has attracted global attention because of increased environmental concentrations, biological toxicity and accumulation in aqueous environments. This study focused on the mechanisms

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