Skip to Content
MilliporeSigma
All Photos(1)

Documents

335789

Sigma-Aldrich

1-Chloro-2,4-difluorobenzene

98%

Sign Into View Organizational & Contract Pricing
All Photos(1)

About This Item

Linear Formula:
ClC6H3F2
CAS Number:
1435-44-5
Molecular Weight:
148.54
MDL number:
MFCD00042569
UNSPSC Code:
12352100
PubChem Substance ID:
24860345
NACRES:
NA.22

Quality Level

100

assay

98%

form

liquid

refractive index

n20/D 1.475 (lit.)

bp

127 °C (lit.)

density

1.353 g/mL at 25 °C (lit.)

SMILES string

Fc1ccc(Cl)c(F)c1

InChI

1S/C6H3ClF2/c7-5-2-1-4(8)3-6(5)9/h1-3H

InChI key

AJCSNHQKXUSMMY-UHFFFAOYSA-N

Related Categories

Application

1-Chloro-2,4-difluorobenzene was used in the preparation of series of benzonorbornadienes. It was also used in the preparation of difluoroarenes.

pictograms

FlameExclamation mark
GHS02,GHS07

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

wgk_germany

WGK 2

flash_point_f

closed cup

flash_point_c

closed cup

ppe

Eyeshields, Faceshields, Gloves, type ABEK (EN14387) respirator filter

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

Jason T Manka et al.
The Journal of organic chemistry, 69(6), 1967-1971 (2004-04-03)
Aryldiazo substituents were used in nucleophilic aromatic substitution reactions of halogens. The Ph-N=N- group activates ortho fluorine atoms toward alkylthiolation under mild conditions. In contrast, the Me(2)N-C(6)H(4)-N=N- group has virtually no activation effect in nucleophilic aromatic substitution, and serves as
K C Caster et al.
The Journal of organic chemistry, 66(9), 2932-2936 (2001-04-28)
This report details the synthesis of several benzonorbornadienes by Diels--Alder cycloaddition of cyclopentadiene derivatives with substituted benzyne intermediates, which were generated by low-temperature metal--halogen exchange of halobenzenes. General conditions were developed, allowing synthesis of most benzonorbornadienes described herein at the

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