Skip to Content
Merck
All Photos(1)

Key Documents

263451

Sigma-Aldrich

1-Bromo-2,6-difluorobenzene

98%

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
BrC6H3F2
CAS Number:
Molecular Weight:
192.99
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

98%

refractive index

n20/D 1.51 (lit.)

functional group

bromo
fluoro

SMILES string

Fc1cccc(F)c1Br

InChI

1S/C6H3BrF2/c7-6-4(8)2-1-3-5(6)9/h1-3H

InChI key

HRZTZLCMURHWFY-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

Three-component coupling reaction of 1-bromo-2,6-difluorobenzene with benzyne and isocyanides has been reported.

Application

1-Bromo-2,6-difluorobenzene has been used in the synthesis of tris(fluorophenyl)boranes.

Pictograms

FlameExclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

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

Target Organs

Respiratory system

Storage Class Code

3 - Flammable liquids

WGK

WGK 3

Flash Point(F)

127.4 °F - closed cup

Flash Point(C)

53 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

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

Visit the Document Library

Three-component coupling of arynes and organic bromides.
Hiroto Yoshida et al.
Angewandte Chemie (International ed. in English), 50(41), 9676-9679 (2011-09-03)
Juan A Nicasio et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 19(33), 11016-11020 (2013-07-03)
An analysis of the metal-free reduction of electron deficient olefins by frustrated Lewis pairs indicates that the rate-determining step might be either the heterolytic cleavage of H2 to form an -onium borohydride salt, or the subsequent transfer of the hydride
Ji Gwang Yu et al.
Chemistry (Weinheim an der Bergstrasse, Germany), 23(63), 16044-16050 (2017-08-24)
Four dibenzofuran-type host materials substituted with a carbazolylcarbazole moiety were synthesized to investigate the effect of substitution position on the material parameters and device performances of host materials. The carbazolylcarbazole moiety was substituted at the 1-, 2-, 3-, and 4-positions

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