Skip to Content
Merck
All Photos(1)

Documents

382957

Sigma-Aldrich

2,6-Difluoronitrobenzene

98%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
F2C6H3NO2
CAS Number:
Molecular Weight:
159.09
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

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

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

190.4 °F - closed cup

Flash Point(C)

88 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

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

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service