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I7632

Sigma-Aldrich

Iodobenzene

98%

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Empirical Formula (Hill Notation):
C6H5I
CAS Number:
Molecular Weight:
204.01
Beilstein:
1446140
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.22

Assay

98%

refractive index

n20/D 1.62 (lit.)

bp

188 °C (lit.)

mp

−29 °C (lit.)

density

1.823 g/mL at 25 °C (lit.)

SMILES string

Ic1ccccc1

InChI

1S/C6H5I/c7-6-4-2-1-3-5-6/h1-5H

InChI key

SNHMUERNLJLMHN-UHFFFAOYSA-N

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This Item
535990101605394602
Iodobenzene 98%

Sigma-Aldrich

I7632

Iodobenzene

Iodobenzene-d5 98 atom % D

Sigma-Aldrich

394602

Iodobenzene-d5

refractive index

n20/D 1.62 (lit.)

refractive index

n20/D 1.504 (lit.)

refractive index

-

refractive index

n20/D 1.6161 (lit.)

bp

188 °C (lit.)

bp

177-179 °C (lit.)

bp

226-227 °C (lit.)

bp

188 °C (lit.)

mp

−29 °C (lit.)

mp

-

mp

53-54 °C (lit.)

mp

-29 °C (lit.)

density

1.823 g/mL at 25 °C (lit.)

density

1.84 g/mL at 25 °C (lit.)

density

-

density

1.868 g/mL at 25 °C

Quality Level

200

Quality Level

200

Quality Level

200

Quality Level

-

General description

Iodobenzene, also known as phenyl iodide, is commonly used as an arylating agent in various cross-coupling reactions.

Application

Iodobenzene is used in various C-C coupling reactions. It can be used in the preparation of iodobenzene dichloride, which is employed as an oxidant to oxidize alcohols to carbonyl compounds and as a chlorinating agent.

Pictograms

Exclamation mark

Signal Word

Warning

Hazard Statements

Precautionary Statements

Hazard Classifications

Acute Tox. 4 Oral

Storage Class Code

10 - Combustible liquids

WGK

WGK 3

Flash Point(F)

170.6 °F - closed cup

Flash Point(C)

77 °C - closed cup

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

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Size effects of PVP- Pd nanoparticles on the catalytic Suzuki reactions in aqueous solution.
Li, Yin et al.
Langmuir, 18(12), 4921-4925 (2002)
Ring-Opening 1, 3-Dichlorination of Donor-Acceptor Cyclopropanes by Iodobenzene Dichloride.
Garve, Lennart KB et al.
Organic Letters, 16(21), 5804-5807 (2014)
Aleksandra A Zagulyaeva et al.
Organic letters, 12(20), 4644-4647 (2010-09-17)
Alkylcarboxamides can be converted to the respective amines by Hofmann rearrangement using hypervalent iodine species generated in situ from PhI and Oxone in aqueous acetonitrile. On the basis of this reaction, a convenient experimental procedure for the preparation of alkylcarbamates
Rainer Wilcken et al.
Journal of computer-aided molecular design, 26(8), 935-945 (2012-08-07)
Halogen bonds are specific embodiments of the sigma hole bonding paradigm. They represent directional interactions between the halogens chlorine, bromine, or iodine and an electron donor as binding partner. Using quantum chemical calculations at the MP2 level, we systematically explore
A universal approach to the synthesis of noble metal nanodendrites and their catalytic properties.
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Angewandte Chemie (International ed. in English), 49(29), 4962-4966 (2010-06-12)

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