Skip to Content
Merck
CN

528897

5-Bromo-2-iodotoluene

98%

Sign In to View Organizational & Contract Pricing.

Select a Size


About This Item

Linear Formula:
CH3C6H3(Br)I
CAS Number:
Molecular Weight:
296.93
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist
Technical Service
Need help? Our team of experienced scientists is here for you.
Let Us Assist

Product Name

5-Bromo-2-iodotoluene, 98%

InChI

1S/C7H6BrI/c1-5-4-6(8)2-3-7(5)9/h2-4H,1H3

SMILES string

Cc1cc(Br)ccc1I

InChI key

GHTUADBHTFHMNI-UHFFFAOYSA-N

assay

98%

refractive index

n20/D 1.65 (lit.)

bp

263 °C (lit.)

density

2.08 g/mL at 25 °C (lit.)

Application

5-Bromo-2-iodotoluene may be used in the synthesis of:
  • 2-bromo-5-(4-bromo-2-methylphenyl)-3-methylpyridine
  • 4-bromo-4′-(carbazol-9-yl)-2-methylbiphenyl
  • 4,4′-dibromo-2-methyl-biphenyl
  • 3-methyl-4-phenylbromobenzene
  • 4-(4-bromo-2-methylphenyl)butanoic acid

General description

5-Bromo-2-iodotoluene is a halogenated hydrocarbon. It undergoes chemoselective Suzuki reaction with phenylboronic acid to yield the corresponding carboxylic acid.

pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

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

target_organs

Respiratory system

Storage Class

10 - Combustible liquids

wgk

WGK 3

flash_point_f

230.0 °F - closed cup

flash_point_c

110 °C - closed cup

ppe

Eyeshields, Gloves, type ABEK (EN14387) respirator filter

Regulatory Information

新产品
This item has

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

Synthesis of new phenylpyridyl scaffolds using the Garlanding approach.
Voisin-Chiret AS, et al.
Tetrahedron, 66(40), 8000-8005 (2010)
Synthesis of comb polyphenylenes by Suzuki coupling from AB macromonomers.
Zhou S, et al.
Journal of Polymer Science Part A: Polymer Chemistry, 52(11), 1519-1524 (2014)
Synthesis, Properties and Applications of Biphenyl Functionalized 9, 9-Bis (4-diphenylaminophenyl) fluorenes as Bifunctional Materials for Organic Electroluminescent Devices.
Thangthong A-M, et al.
European Journal of Organic Chemistry, 27, 5263-5274 (2012)
M Jonathan Fray et al.
Journal of medicinal chemistry, 46(16), 3514-3525 (2003-07-25)
The pathology of chronic dermal ulcers is characterized by excessive proteolytic activity which degrades extracellular matrix (required for cell migration) and growth factors and their receptors. The overexpression of MMP-3 (stromelysin-1) and MMP-13 (collagenase-3) is associated with nonhealing wounds, whereas
E Scott Priestley et al.
Journal of medicinal chemistry, 58(15), 6225-6236 (2015-07-08)
On the basis of a crystal structure of a phenylpyrrolidine lead and subsequent molecular modeling results, we designed and synthesized a novel series of macrocyclic FVIIa inhibitors. The optimal 16-membered macrocycle was 60-fold more potent than an acyclic analog. Further

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