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162302

Sigma-Aldrich

1-Chloro-2-fluorobenzene

99%

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About This Item

Linear Formula:
ClC6H4F
CAS Number:
348-51-6
Molecular Weight:
130.55
EC Number:
206-476-8
MDL number:
MFCD00000533
UNSPSC Code:
12352100
PubChem Substance ID:
24849976
NACRES:
NA.22

Assay

99%

form

liquid

refractive index

n20/D 1.501 (lit.)

bp

137-138 °C (lit.)

mp

−43-−42 °C (lit.)

density

1.244 g/mL at 25 °C (lit.)

SMILES string

Fc1ccccc1Cl

InChI

1S/C6H4ClF/c7-5-3-1-2-4-6(5)8/h1-4H

InChI key

ZCJAYDKWZAWMPR-UHFFFAOYSA-N

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Application

1-Chloro-2-fluorobenzene was used in the 9F NMR analysis of conversion of 3,4-fluoro- and 3-chloro-4-fluoroaniline by Rhodococcus sp. strain. It was used in microwave-assisted traceless rapid synthesis of benzimidazolones on Ameba resin.

Pictograms

FlameExclamation mark
GHS02,GHS07

Signal Word

Warning

Hazard Statements

H226,H315,H319

Hazard Classifications

Eye Irrit. 2 - Flam. Liq. 3 - Skin Irrit. 2

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

87.8 °F - closed cup

Flash Point(C)

31 °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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Haifeng Chen et al.
Chemosphere, 146, 32-39 (2015-12-29)
Halonitromethanes (HNMs), as an emerging class of disinfection by-products containing nitrogen (N-DBPs) in drinking water, have possessed public health concerns. Two most studied materials, graphene and nanometer-sized zero-valent iron, have been successfully combined into binary nanocomposites (G-nZVI) via facile carbonization
Microwave-assisted traceless synthesis of benzimidazolones.
Xu X-J and Zong Y-X.
Tetrahedron Letters, 48(1), 129-132 (2007)
Vasili Travkin et al.
FEMS microbiology letters, 209(2), 307-312 (2002-05-15)
In this paper we report the isolation and characterization of an anaerobic enrichment culture as well as of a Rhodococcus sp. strain 2 capable of degrading 3,4-dihaloanilines under nitrate reducing conditions. Using mass spectrometry several of the intermediates formed in

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