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Sigma-Aldrich

1,2-Difluorobenzene

98%

Synonym(s):

o-Difluorobenzene

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About This Item

Empirical Formula (Hill Notation):
C6H4F2
CAS Number:
Molecular Weight:
114.09
Beilstein:
1905113
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

form

liquid

refractive index

n20/D 1.443 (lit.)

bp

92 °C (lit.)

mp

−34 °C (lit.)

density

1.158 g/mL at 25 °C (lit.)

SMILES string

Fc1ccccc1F

InChI

1S/C6H4F2/c7-5-3-1-2-4-6(5)8/h1-4H

InChI key

GOYDNIKZWGIXJT-UHFFFAOYSA-N

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General description

1,2-Difluorobenzene undergoes defluorination under very mild conditions by H2 in the presence of NaOAc over rhodium pyridylphosphine and bipyridyl complexes tethered on a silica-supported palladium catalyst.

Application

1,2-Difluorobenzene(1,2-DFB) has been used to study the mechanism of dissociation of o-, m- and p-difluorobenzene ions by threshold photoelectron photoion coincidence spectroscopy. It has been used to study the room temperature adsorption of 1,2-DFB, 1,2-dichlorobenzene and 1,2-dibromobenzene on Si(100)2x1 by X-ray photoelectron spectroscopy and temperature programmed desorption. It was used as solvent in electrochemical studies on transition metal complexes.
Solvent useful for electrochemical studies on transition metal complexes.

Pictograms

Flame

Signal Word

Danger

Hazard Statements

Precautionary Statements

Hazard Classifications

Flam. Liq. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

33.8 °F - closed cup

Flash Point(C)

1 °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’.

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Hydrodefluorination of fluorobenzene and 1, 2-difluorobenzene under mild conditions over rhodium pyridylphosphine and bipyridyl complexes tethered on a silica-supported palladium catalyst.
Yang H, et al.
Organometallics, 18(12), 2285-2287 (1999)
Competition between associative and dissociative adsorption of 1, 2-dihalogenated benzenes on Si (100) 2? 1: Formation of dihalocyclohexadiene, halophenyl and phenylene adstructures.
Zhou XJ and Leung KT.
Surface Science, 600(16), 3285-3296 (2006)
I M Rietjens et al.
Biochemistry, 32(18), 4801-4812 (1993-05-11)
In the present study, a hypothesis is presented for the prediction of the regioselectivity of cytochrome P-450 catalyzed hydroxylation of fluorobenzenes. The regioselectivity of the in vivo hydroxylation of fluorobenzene, 1,2-difluorobenzene, 1,3-difluorobenzene, 1,2,3-triluorobenzene, and 1,2,4-triflurobenzene could be predicted within 6%
Inorganic Chemistry, 28, 3923-3923 (1989)
Adrian Romero-Flores et al.
Chemosphere, 186, 151-159 (2017-08-05)
Electronic noses have been widely used in the food industry to monitor process performance and quality control, but use in wastewater and biosolids treatment has not been fully explored. Therefore, we examined the feasibility of an electronic nose to discriminate

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