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Sigma-Aldrich

2,6-Difluoronitrobenzene

98%

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About This Item

Linear Formula:
F2C6H3NO2
CAS Number:
19064-24-5
Molecular Weight:
159.09
EC Number:
242-793-8
MDL number:
MFCD00192035
UNSPSC Code:
12352100
PubChem Substance ID:
24863927
NACRES:
NA.22

assay

98%

form

solid

refractive index

n20/D 1.494 (lit.)

bp

91-92 °C/11 mmHg (lit.)

density

1.503 g/mL at 25 °C (lit.)

SMILES string

[O-][N+](=O)c1c(F)cccc1F

InChI

1S/C6H3F2NO2/c7-4-2-1-3-5(8)6(4)9(10)11/h1-3H

InChI key

SSNCMIDZGFCTST-UHFFFAOYSA-N

General description

2,6-Difluoronitrobenzene is an organic building block. Molecular structure, conformation and potential to internal rotation of 2,6-difluoronitrobenzene been studied by gas-phase electron diffraction (GED), MP2 ab initio, and by B3LYP density functional calculations.

Application

2,6-Difluoronitrobenzene may be used in the preparation of secondary amine precursors, required for the synthesis of two families of nitric oxide donors.

pictograms

Exclamation mark
GHS07

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

Storage Class

11 - Combustible Solids

wgk_germany

WGK 3

flash_point_f

190.4 °F - closed cup

flash_point_c

88 °C - closed cup

ppe

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

Certificates of Analysis (COA)

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Brandon Curtis et al.
Bioorganic & medicinal chemistry, 21(5), 1123-1135 (2013-02-05)
Atherosclerosis, a leading cause of death worldwide, is associated with the excessive proliferation of vascular smooth muscle cells. Nitrogen monoxide, more commonly known as nitric oxide, inhibits this uncontrolled proliferation. Herein we report the preparation of two families of nitric
Olga V Dorofeeva et al.
The journal of physical chemistry. A, 112(22), 5002-5009 (2008-05-09)
3,5-Difluoronitrobenzene (3,5-DFNB) and 2,6-difluoronitrobenzene (2,6-DFNB) have been studied by gas-phase electron diffraction (GED), MP2 ab initio, and by B3LYP density functional calculations. Refinements of r h1 and r e static and r h1 dynamic GED models were carried out for

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