Skip to Content
Merck
All Photos(1)

Documents

280097

Sigma-Aldrich

3-Bromoiodobenzene

98%

Synonym(s):

1-Bromo-3-iodobenzene, 1-Iodo-3-bromobenzene, 3-Bromo-1-iodobenzene, 3-Bromophenyl iodide, 3-Iodo-1-bromobenzene, 3-Iodobromobenzene, 3-Iodophenyl bromide, m-Bromoiodobenzene

Sign Into View Organizational & Contract Pricing


About This Item

Linear Formula:
BrC6H4I
CAS Number:
Molecular Weight:
282.90
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

98%

form

liquid

contains

copper as stabilizer

refractive index

n20/D 1.66 (lit.)

bp

120 °C/18 mmHg (lit.)

mp

−9.3-−9 °C (lit.)

density

2.219 g/mL at 25 °C (lit.)

SMILES string

Brc1cccc(I)c1

InChI

1S/C6H4BrI/c7-5-2-1-3-6(8)4-5/h1-4H

InChI key

CTPUUDQIXKUAMO-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

Application

3-Bromoiodobenzene has been used in the preparation of:
  • 1-(3′-bromophenyl)-3,3,4,4,5,5,6,6,7,7,8,8,9,9,10,10,10-heptadecafluorodec-1-ene
  • 1-(3′-bromophenyl)-3,3,4,4,5,5,6,6,7,7,8,8,8-tridecafluorooct-1-ene
  • oxygen-tethered 1,6-enynes

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

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

235.4 °F - closed cup

Flash Point(C)

113 °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

Alexandre Pradal et al.
Beilstein journal of organic chemistry, 7, 1021-1029 (2011-09-15)
A comprehensive study on the asymmetric gold-catalyzed cycloisomerization reaction of heteroatom tethered 1,6-enynes is described. The cycloisomerization reactions were conducted in the presence of the chiral cationic Au(I) catalyst consisting of (R)-4-MeO-3,5-(t-Bu)(2)-MeOBIPHEP-(AuCl)(2) complex and silver salts (AgOTf or AgNTf(2)) in
Efficient access to perfluoroalkylated aryl compounds by Heck reaction.
Darses S, et al.
European Journal of Organic Chemistry, 2001(6), 1121-1128 (2001)
Junpei Miyake et al.
Science advances, 3(10), eaao0476-eaao0476 (2017-10-28)
Proton exchange membrane fuel cells (PEMFCs) are promising devices for clean power generation in automotive, stationary, and portable applications. Perfluorosulfonic acid (PFSA) ionomers (for example, Nafion) have been the benchmark PEMs; however, several problems, including high gas permeability, low thermal

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